chr_pos SNPID A1 A2 OR.A1. P.val OR_95.CIup.OR_95.CIlow beta se zscore id rm_id snp_id modification_type species strand 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 6_29827788 rs1611700 T C 0.91 1.4e-12 0.93-0.89 -0.0943106794712413 0.0133130993702645 -7.08405134283675 1374203 RMVar_ID_1374203 Human_SNP_ID_271539647 m6A Human - 29827786 29827786 CCGGGTGGGTGAGCGAGGACTTTAGAACCAGGACCGCGGCGACGCTGATTGGCTTCTCTAAAAAC CCGGGTGGGTGAGCGAGGACTTTAGAACCAGGACTGCGGCGACGCTGATTGGCTTCTCTAAAAAC G A HCG4P8 Ensembl:ENSG00000229142 Pseudogene exon - - - - Prediction:(Low) rs752110494 Functional Gain SNV dbSNP153 35..35 33 - - - 6_29944796 rs2894002 T C 0.89 1.3e-12 0.92-0.86 -0.116533816255952 0.0164263816436337 -7.09430833789958 287788 RMVar_ID_287788 Human_SNP_ID_271575819 m6A Human + 29944796 29944796 ACTCTTTTGTAAAGCACCTGTTAAAATGAAGGACAGATTTATCACCTTGATTACGGCGGTGATGG ACTCTTTTGTAAAGCACCTGTTAAAATGAAGGCCAGATTTATCACCTTGATTACGGCGGTGATGG A C HLA-A Ensembl:ENSG00000206503 Protein coding intron GSE122948:GSM3489019,GSM3489020 HEK293T,PCIF1_KO - 31279658 miCLIP:(High) rs1238950429 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_660486 6_30108111 rs9261481 T C 1.24 1.2e-40 1.28-1.20 0.215111379616945 0.0161143818274372 13.3490308173463 1536661 RMVar_ID_1536661 Human_SNP_ID_866890783 m6A Human - 30108112 30108112 CCAACCCCTGTTCCTCTGGAACTGGAGAAAAAACTCAGTGAAGCAAAATCAAGACATGACTCCAT CCAACCCCTGTTCCTCTGGAACTGGAGAAAAGACTCAGTGAAGCAAAATCAAGACATGACTCCAT T C TRIM31 Ensembl:ENSG00000204616 Protein coding CDS - - - - Prediction:(Low) - Functional Gain SNV TCGA 32..32 33 COAD 1 - Human_Splice_Rec_748174,Human_Splice_Rec_748175,Human_Splice_Rec_748181,Human_Splice_Rec_748194,Human_Splice_Rec_748195 6_30914496 rs58893284 T G 0.88 9.4e-10 0.92-0.84 -0.127833371509885 0.0208902686438355 -6.11927848747926 1376587 RMVar_ID_1376587 Human_SNP_ID_271808131 m6A Human + 30914500 30914500 GTGCAGGTGGAGATCGCCGCGGCCCTGGCGGGACTCCTTGCTGGCTCTTGGGCGCGCTGATGCCC GTGCAGGTGGAGATCGCCGCGGCCCTGGCGGGACTCTTTGCTGGCTCTTGGGCGCGCTGATGCCC C T AL669830.2,VARS2 Ensembl:ENSG00000288473,Ensembl:ENSG00000137411 lincRNA,Protein coding exon,5'UTR - - - - Prediction:(Low) rs1264305 Functional Gain SNV dbSNP153,EGP 37..37 33 - - - Human_RBP_ID_267188,Human_RBP_ID_5400338,Human_RBP_ID_9354687 GWAS_ID_156924,GWAS_ID_156925,GWAS_ID_156926,GWAS_ID_156927,GWAS_ID_156928,GWAS_ID_156929,GWAS_ID_156930,GWAS_ID_156931,GWAS_ID_156932,GWAS_ID_156933 6_30914496 rs58893284 T G 0.88 9.4e-10 0.92-0.84 -0.127833371509885 0.0208902686438355 -6.11927848747926 1376586 RMVar_ID_1376586 Human_SNP_ID_271808130 m6A Human + 30914499 30914501 GTGCAGGTGGAGATCGCCGCGGCCCTGGCGGGACTCCTTGCTGGCTCTTGGGCGCGCTGATGCCC GTGCAGGTGGAGATCGCCGCGGCCCTGGCGGGACTC__TGCTGGCTCTTGGGCGCGCTGATGCCC CCT C AL669830.2,VARS2 Ensembl:ENSG00000288473,Ensembl:ENSG00000137411 lincRNA,Protein coding exon,5'UTR - - - - Prediction:(Low) rs1423055476 Functional Gain DEL dbSNP153 37..38 33 - - - Human_RBP_ID_267188,Human_RBP_ID_5400338,Human_RBP_ID_9354687 6_31034920 rs9262668 T C 0.83 2.2e-22 0.86-0.80 -0.186329578191493 0.0191458727373859 -9.73210157339288 1376776 RMVar_ID_1376776 Human_SNP_ID_271840485 m6A Human + 31034922 31034922 GGCTACGGAGTGAATCATGGCGGGCATTATGGACATGGAGGAGGCCACTGAGGACACCATGGAGT GGCTACGGAGTGAATCATGGCGGGCATTATGGACCTGGAGGAGGCCACTGAGGACACCATGGAGT A C MUC22 Ensembl:ENSG00000261272 Protein coding CDS - - - - Prediction:(Low) rs756901630 Functional Loss SNV dbSNP153 35..35 33 - - - 6_31165846 rs28397282 T C 1.16 3.2e-25 1.20-1.13 0.148420005118273 0.0143046353523256 10.3756580620661 1376927 RMVar_ID_1376927 Human_SNP_ID_271873106 m6A Human - 31165843 31165843 TCCCTGAACCTAGTGGGGAGGGGCAGGGGCAGACT___ACCCTCACCCATGAAGAGGAGTAGGGA TCCCTGAACCTAGTGGGGAGGGGCAGGGGCAGACTCTAACCCTCACCCATGAAGAGGAGTAGGGA T TTAG POU5F1 Ensembl:ENSG00000204531 Protein coding intron - - - - Prediction:(Low) rs1554134963 Functional Gain INS dbSNP153 36..38 33 - - - 6_31203132 chr6:31203132 A G 0.62 3.1e-16 0.70-0.56 -0.478035800943 0.0585156149186326 -8.16937157043843 1376983 RMVar_ID_1376983 Human_SNP_ID_271882746 m6A Human + 31203151 31203151 CCAAGCCCAGGAAAGTGAAAAGAGAAGCAGGAACAGTAAAATACTCCACAGG_AAAGAAAAATCT CCAAGCCCAGGAAAGTGAAAAGAGAAGCAGGAACAGTAAAATACTCCACAGGAAAAGAAAAATCT G GA HCG27 Ensembl:ENSG00000206344 lincRNA exon - - - - Prediction:(Low) rs35578787 Functional Gain INS dbSNP153 53..53 33 - - - Human_RBP_ID_5621418 RMVar_hsa_circ_95727,RMVar_hsa_circ_237822 6_31276245 rs6911704 A G 0.84 2.1e-20 0.87-0.81 -0.174353387144778 0.0188344960952836 -9.25713044101232 1377016 RMVar_ID_1377016 Human_SNP_ID_271902698 m6A Human + 31276248 31276248 TGAAAGATGCACTTTTCAAGTGGGAAAGTAAGACTGTCCTGTGCAATGGGCCTTGGGCTTTGGTT TGAAAGATGCACTTTTCAAGTGGGAAAGTAAGACTTTCCTGTGCAATGGGCCTTGGGCTTTGGTT G T USP8P1 Ensembl:ENSG00000214892 Pseudogene exon - - - - Prediction:(Low) rs1562035936 Functional Loss SNV dbSNP153 36..36 33 - - - 6_31276245 rs6911704 A G 0.84 2.1e-20 0.87-0.81 -0.174353387144778 0.0188344960952836 -9.25713044101232 1377015 RMVar_ID_1377015 Human_SNP_ID_271902697 m6A Human + 31276244 31276244 TGAAAGATGCACTTTTCAAGTGGGAAAGTAAGACTGTCCTGTGCAATGGGCCTTGGGCTTTGGTT TGAAAGATGCACTTTTCAAGTGGGAAAGTAAAACTGTCCTGTGCAATGGGCCTTGGGCTTTGGTT G A USP8P1 Ensembl:ENSG00000214892 Pseudogene exon - - - - Prediction:(Low) rs2524074 Functional Loss SNV dbSNP153 32..32 33 - - - GWAS_ID_157358,GWAS_ID_157359,GWAS_ID_157360,GWAS_ID_157361,GWAS_ID_157362,GWAS_ID_157363,GWAS_ID_157364,GWAS_ID_157365,GWAS_ID_157366,GWAS_ID_157367,GWAS_ID_157368,GWAS_ID_157369,GWAS_ID_157370,GWAS_ID_157371,GWAS_ID_157372,GWAS_ID_157373,GWAS_ID_157374,GWAS_ID_157375,GWAS_ID_157376,GWAS_ID_157377,GWAS_ID_157378,GWAS_ID_157379,GWAS_ID_157380,GWAS_ID_157381,GWAS_ID_157382,GWAS_ID_157383,GWAS_ID_157384,GWAS_ID_157385,GWAS_ID_157386,GWAS_ID_157387,GWAS_ID_157388,GWAS_ID_157389,GWAS_ID_157390,GWAS_ID_157391,GWAS_ID_157392,GWAS_ID_157393,GWAS_ID_157394,GWAS_ID_157395,GWAS_ID_157396,GWAS_ID_157397,GWAS_ID_157398,GWAS_ID_157399,GWAS_ID_157400,GWAS_ID_157401,GWAS_ID_157402,GWAS_ID_157403,GWAS_ID_157404,GWAS_ID_157405,GWAS_ID_157406,GWAS_ID_157407,GWAS_ID_157408,GWAS_ID_157409,GWAS_ID_157410,GWAS_ID_157411,GWAS_ID_157412,GWAS_ID_157413,GWAS_ID_157414,GWAS_ID_157415,GWAS_ID_157416,GWAS_ID_157417,GWAS_ID_157418,GWAS_ID_157419,GWAS_ID_157420,GWAS_ID_157421,GWAS_ID_157422,GWAS_ID_157423,GWAS_ID_157424,GWAS_ID_157425,GWAS_ID_157426,GWAS_ID_157427,GWAS_ID_157428,GWAS_ID_157429,GWAS_ID_157430,GWAS_ID_157431,GWAS_ID_157432,GWAS_ID_157433,GWAS_ID_157434,GWAS_ID_157435,GWAS_ID_157436,GWAS_ID_157437,GWAS_ID_157438,GWAS_ID_157439,GWAS_ID_157440,GWAS_ID_157441,GWAS_ID_157442,GWAS_ID_157443,GWAS_ID_157444,GWAS_ID_157445,GWAS_ID_157446,GWAS_ID_157447,GWAS_ID_157448,GWAS_ID_157449,GWAS_ID_157450,GWAS_ID_157451,GWAS_ID_157452,GWAS_ID_157453,GWAS_ID_157454,GWAS_ID_157455,GWAS_ID_157456,GWAS_ID_157457,GWAS_ID_157458,GWAS_ID_157459,GWAS_ID_157460,GWAS_ID_157461,GWAS_ID_157462,GWAS_ID_157463,GWAS_ID_157464,GWAS_ID_157465,GWAS_ID_157466,GWAS_ID_157467,GWAS_ID_157468,GWAS_ID_157469,GWAS_ID_157470,GWAS_ID_157471,GWAS_ID_157472,GWAS_ID_157473,GWAS_ID_157474,GWAS_ID_157475,GWAS_ID_157476,GWAS_ID_157477,GWAS_ID_157478,GWAS_ID_157479,GWAS_ID_157480,GWAS_ID_157481,GWAS_ID_157482,GWAS_ID_157483,GWAS_ID_157484,GWAS_ID_157485,GWAS_ID_157486,GWAS_ID_157487,GWAS_ID_157488,GWAS_ID_157489,GWAS_ID_157490,GWAS_ID_157491,GWAS_ID_157492,GWAS_ID_157493,GWAS_ID_157494,GWAS_ID_157495,GWAS_ID_157496,GWAS_ID_157497,GWAS_ID_157498,GWAS_ID_157499,GWAS_ID_157500,GWAS_ID_157501,GWAS_ID_157502,GWAS_ID_157503,GWAS_ID_157504,GWAS_ID_157505,GWAS_ID_157506,GWAS_ID_157507,GWAS_ID_157508,GWAS_ID_157509,GWAS_ID_157510,GWAS_ID_157511,GWAS_ID_157512,GWAS_ID_157513,GWAS_ID_157514,GWAS_ID_157515,GWAS_ID_157516,GWAS_ID_157517,GWAS_ID_157518,GWAS_ID_157519 6_31276245 rs6911704 A G 0.84 2.1e-20 0.87-0.81 -0.174353387144778 0.0188344960952836 -9.25713044101232 1377017 RMVar_ID_1377017 Human_SNP_ID_271902703 m6A Human + 31276264 31276264 TGAAAGATGCACTTTTCAAGTGGGAAAGTAAGACTGTCCTGTGCAATGGGCCTTGGGCTTTGGTT TGAAAGATGCACTTTTCAAGTGGGAAAGTAAGACTGTCCTGTGCAATGGGCTTTGGGCTTTGGTT C T USP8P1 Ensembl:ENSG00000214892 Pseudogene exon - - - - Prediction:(Low) rs1269418861 Functional Loss SNV dbSNP153 52..52 33 - - - 6_31276245 rs6911704 A G 0.84 2.1e-20 0.87-0.81 -0.174353387144778 0.0188344960952836 -9.25713044101232 1377018 RMVar_ID_1377018 Human_SNP_ID_271902708 m6A Human + 31276274 31276274 TGAAAGATGCACTTTTCAAGTGGGAAAGTAAGACTGTCCTGTGCAATGGGCCTTGGGCTTTGGTT TGAAAGATGCACTTTTCAAGTGGGAAAGTAAGACTGTCCTGTGCAATGGGCCTTGGGCTTTTGTT G T USP8P1 Ensembl:ENSG00000214892 Pseudogene exon - - - - Prediction:(Low) rs367665188 Functional Loss SNV dbSNP153 62..62 33 - - - 6_31281491 rs36004907 T G 1.27 5.7e-38 1.31-1.22 0.2390169004705 0.0185546378640558 12.8817874119508 1377053 RMVar_ID_1377053 Human_SNP_ID_271903891 m6A Human + 31281493 31281493 GAAGAAAGCATTCATGGGACCACTCAAGAAAGACCGAATTGCAAAGGAAGAAGGAGCTTAATGCT GAAGAAAGCATTCATGGGACCACTCAAGAAAGACTGAATTGCAAAGGAAGAAGGAGCTTAATGCT C T RPL3P2 Ensembl:ENSG00000227939 Pseudogene exon - - - - Prediction:(Low) rs560577518 Functional Gain SNV dbSNP153 35..35 33 - - - Human_miRNA_ID_1875943 6_31301636 rs28752871 T G 0.76 1.2e-19 0.80-0.71 -0.27443684570176 0.0302606358564121 -9.06910373608718 1377079 RMVar_ID_1377079 Human_SNP_ID_271908364 m6A Human - 31301636 31301636 CCATAGCCTAAGTGTATGCTTCATCCTGAAGGACATTACCCATCCTGATAGGATGTGATCTTCAA CCATAGCCTAAGTGTATGCTTCATCCTGAAGGGCATTACCCATCCTGATAGGATGTGATCTTCAA T C HLA-B,LINC02571 Ensembl:ENSG00000234745,Ensembl:ENSG00000256166 Protein coding,lincRNA intron,exon - - - - Prediction:(Low) rs1025676788 Functional Loss SNV dbSNP153 33..33 33 - - - 6_31301636 rs28752871 T G 0.76 1.2e-19 0.80-0.71 -0.27443684570176 0.0302606358564121 -9.06910373608718 1377077 RMVar_ID_1377077 Human_SNP_ID_271908356 m6A Human - 31301604 31301604 CCATAGCCTAAGTGTATGCTTCATCCTGAAGGACATTACCCATCCTGATAGGATGTGATCTTCAA CCATAGCCTAAGTGTATGCTTCATCCTGAAGGACATTACCCATCCTGATAGGATGTGATCTTCAG T C HLA-B,LINC02571 Ensembl:ENSG00000234745,Ensembl:ENSG00000256166 Protein coding,lincRNA intron,exon - - - - Prediction:(Low) rs1362227727 Functional Loss SNV dbSNP153 65..65 33 - - - 6_31301636 rs28752871 T G 0.76 1.2e-19 0.80-0.71 -0.27443684570176 0.0302606358564121 -9.06910373608718 1377078 RMVar_ID_1377078 Human_SNP_ID_271908362 m6A Human - 31301629 31301629 CCATAGCCTAAGTGTATGCTTCATCCTGAAGGACATTACCCATCCTGATAGGATGTGATCTTCAA CCATAGCCTAAGTGTATGCTTCATCCTGAAGGACATTACTCATCCTGATAGGATGTGATCTTCAA G A HLA-B,LINC02571 Ensembl:ENSG00000234745,Ensembl:ENSG00000256166 Protein coding,lincRNA intron,exon - - - - Prediction:(Low) rs774051270 Functional Loss SNV dbSNP153 40..40 33 - - - 6_31357210 chr6:31357210 G C 0.77 5.1e-18 0.82-0.73 -0.261364764134408 0.0302116956541654 -8.65111204370194 1377113 RMVar_ID_1377113 Human_SNP_ID_271925522 m6A Human + 31357214 31357214 CTGAGTCCGGGTGGGTGCGTGGGGACTTTAGAACTGGGACCGCGGCGACGCTGATTGGCTTCTCT CTGAGTCCGGGTGGGTGCGTGGGGACTTTAGAACTGTGACCGCGGCGACGCTGATTGGCTTCTCT G T AL671883.2 Ensembl:ENSG00000271581 Pseudogene exon - - - - Prediction:(Low) rs1490535166 Functional Gain SNV dbSNP153 37..37 33 - - - 6_31380807 rs2857282 A T 0.78 7.4e-40 0.81-0.75 -0.2484613592985 0.0188045680609731 -13.2128192731082 1377124 RMVar_ID_1377124 Human_SNP_ID_271931393 m6A Human + 31380803 31380803 ATGGAGCTGGAGAAGGAGTTGTTAGATCAGGGACAAATAACCATGTTATAGTGGCAACAGGAAAT ATGGAGCTGGAGAAGGAGTTGTTAGATCGGGGACAAATAACCATGTTATAGTGGCAACAGGAAAT A G ZDHHC20P2 Ensembl:ENSG00000223702 Pseudogene exon - - - - Prediction:(Low) rs9266689 Functional Loss SNV dbSNP153 29..29 33 - - - GWAS_ID_157814,GWAS_ID_157815,GWAS_ID_157816,GWAS_ID_157817,GWAS_ID_157818,GWAS_ID_157819,GWAS_ID_157820,GWAS_ID_157821,GWAS_ID_157822,GWAS_ID_157823,GWAS_ID_157824,GWAS_ID_157825,GWAS_ID_157826,GWAS_ID_157827,GWAS_ID_157828,GWAS_ID_157829,GWAS_ID_157830,GWAS_ID_157831,GWAS_ID_157832,GWAS_ID_157833,GWAS_ID_157834 6_31380807 rs2857282 A T 0.78 7.4e-40 0.81-0.75 -0.2484613592985 0.0188045680609731 -13.2128192731082 1377125 RMVar_ID_1377125 Human_SNP_ID_271931394 m6A Human + 31380806 31380806 ATGGAGCTGGAGAAGGAGTTGTTAGATCAGGGACAAATAACCATGTTATAGTGGCAACAGGAAAT ATGGAGCTGGAGAAGGAGTTGTTAGATCAGGAACAAATAACCATGTTATAGTGGCAACAGGAAAT G A ZDHHC20P2 Ensembl:ENSG00000223702 Pseudogene exon - - - - Prediction:(Low) rs1315403935 Functional Loss SNV dbSNP153 32..32 33 - - - 6_31395209 chr6:31395209 T C 1.23 4e-20 1.28-1.18 0.207014169384326 0.0225307879307723 9.18805724950208 362367 RMVar_ID_362367 Human_SNP_ID_271935132 m6A Human - 31395207 31395207 TGTGCACCTGTGCTTTTATTTCAGGAGCTGGGACAGTTATATTCATCAGAACAGCACGGTGTCAA TGTGCACCTGTGCTTTTATTTCAGGAGCTGGGACGGTTATATTCATCAGAACAGCACGGTGTCAA T C AL645933.3 Ensembl:ENSG00000272221 lincRNA exon GSE122948:GSM3489019,GSM3489020 HEK293T,PCIF1_KO - 31279658 miCLIP:(High) rs1228701590 Functional Loss SNV dbSNP153 35..35 33 - - - Human_RBP_ID_7591929,Human_RBP_ID_15785353 Human_miRNA_ID_3184134 6_32086092 rs204889 A G 0.56 1.2e-29 0.62-0.51 -0.579818495252942 0.0512757709837325 -11.3078454819703 1378198 RMVar_ID_1378198 Human_SNP_ID_272111365 m6A Human - 32086113 32086113 TCCCAGGGTCCTCACCCTTGGGCCTCTTGGGGACTACCGATGAGCCTCCTCCCTCAGGCCCCTCG TCCCAGGGTCCGCACCCTTGGGCCTCTTGGGGACTACCGATGAGCCTCCTCCCTCAGGCCCCTCG A C TNXB Ensembl:ENSG00000168477 Protein coding CDS - - - - Prediction:(Low) rs1451747427 Functional Gain SNV dbSNP153 12..12 33 - - - Human_Splice_Rec_757492,Human_Splice_Rec_757580,Human_Splice_Rec_757666 RMVar_hsa_circ_265629,RMVar_hsa_circ_363169 6_32129434 rs12524510 A G 1.2 1.6e-23 1.24-1.16 0.182321556793955 0.0182409520033362 9.99517770567066 363354 RMVar_ID_363354 Human_SNP_ID_272122314 m6A Human - 32129434 32129434 CAAGAAGATCGTAATCCGTGGCCATGGCTTGGACAAACCCAAACTAGGCTCCTGCTGCCGGGTAC CAAGAAGATCGTAATCCGTGGCCATGGCTTGGGCAAACCCAAACTAGGCTCCTGCTGCCGGGTAC T C FKBPL Ensembl:ENSG00000204315 Protein coding CDS GSE137675:GSM4084045,GSM4084044,GSE52600:GSM1272358,GSM1272357,GSE122948:GSM3489018,GSE122948:GSM3489019,GSM3489020 Ocular melanoma cell line,PIG1 cell line;embryonic stem (ES) cell,H1A T0;HEK293T,Wild type;HEK293T,PCIF1_KO chr6:32128756..32130006,chr6:32128726..32129752 31722709,25456834,31279658 miCLIP:(High) rs747095122 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8900387 6_32188943 rs2071282 A G 2.04 7.3e-85 2.19-1.90 0.712949807856125 0.0365224600158688 19.5208594258534 1378370 RMVar_ID_1378370 Human_SNP_ID_272136810 m6A Human - 32188939 32188939 CCCATGCTCTGGGAGCTGATCTTTTCCCAAGAACTCCTCATTCCACCCCCAACTCATTCCACCCC CCCATGCTCTGGGAGCTGATCTTTTCCCAAGAACTCTTCATTCCACCCCCAACTCATTCCACCCC G A PBX2 Ensembl:ENSG00000204304 Protein coding intron - - - - Prediction:(Low) rs1190035006 Functional Gain SNV dbSNP153 37..37 33 - - - Human_RBP_ID_17091186,Human_RBP_ID_18958207 6_32196313 rs378088 T C 0.75 1.8e-72 0.77-0.73 -0.287682072451781 0.015978448161291 -18.0043812482812 1378414 RMVar_ID_1378414 Human_SNP_ID_272138747 m6A Human - 32196286 32196290 TAAAGATGCCCAGGACAACAGGGTTAGATGGGACAGAGGGCTTCCCACAAAACAGTCAGGCGCAC TAAAGATGCCCAGGACAACAGGGTTAGATGGGACAGAGGGCTTCCCACAAAACAG____GCGCAC CCTGA C NOTCH4 Ensembl:ENSG00000204301 Protein coding exon - - - - Prediction:(Low) rs775859701 Functional Gain DEL dbSNP153 56..59 33 - - - 6_32196313 rs378088 T C 0.75 1.8e-72 0.77-0.73 -0.287682072451781 0.015978448161291 -18.0043812482812 1378415 RMVar_ID_1378415 Human_SNP_ID_272138761 m6A Human - 32196310 32196310 TAAAGATGCCCAGGACAACAGGGTTAGATGGGACAGAGGGCTTCCCACAAAACAGTCAGGCGCAC TAAAGATGCCCAGGACAACAGGGTTAGATGGGACAAAGGGCTTCCCACAAAACAGTCAGGCGCAC C T NOTCH4 Ensembl:ENSG00000204301 Protein coding exon - - - - Prediction:(Low) rs557632279 Functional Gain SNV dbSNP153 36..36 33 - - - 6_33163451 rs6531 A G 0.9 1.4e-10 0.93-0.87 -0.105360515657826 0.016421801303647 -6.41589273366909 363930 RMVar_ID_363930 Human_SNP_ID_272405559 m6A Human + 33163452 33163452 TTTAAATAAGGGTCTCAGCTCTCTAACGGGTAACAGGCTCCAGGTGGGAGGGCCAAGAGCCCCAG TTTAAATAAGGGTCTCAGCTCTCTAACGGGTAAAAGGCTCCAGGTGGGAGGGCCAAGAGCCCCAG C A - - Other Unknown CRA001315:CRX037641,CRX037640 Cerebellum,Cerebellum-5-3 chr6:33163179..33163580 31676230 MeRIP-seq:(Medium) rs1452027676 Functional Loss SNV dbSNP153 34..34 33 - - - 6_33163451 rs6531 A G 0.9 1.4e-10 0.93-0.87 -0.105360515657826 0.016421801303647 -6.41589273366909 363931 RMVar_ID_363931 Human_SNP_ID_272405560 m6A Human + 33163452 33163452 TTTAAATAAGGGTCTCAGCTCTCTAACGGGTAACAGGCTCCAGGTGGGAGGGCCAAGAGCCCCAG TTTAAATAAGGGTCTCAGCTCTCTAACGGGTAATAGGCTCCAGGTGGGAGGGCCAAGAGCCCCAG C T - - Other Unknown CRA001315:CRX037641,CRX037640 Cerebellum,Cerebellum-5-3 chr6:33163179..33163580 31676230 MeRIP-seq:(Medium) rs1452027676 Functional Loss SNV dbSNP153 34..34 33 - - - 6_33403708 chr6:33403708 T C 1.2 1.8e-19 1.25-1.15 0.182321556793955 0.0202022496915529 9.0248145418274 364332 RMVar_ID_364332 Human_SNP_ID_272469350 m6A Human - 33403708 33403708 GAACACCTGATGCTAAGATGAACACAGAAAGGACAAAGGTCAGTGAAGTCTAGGCTCTCTATCCC GAACACCTGATGCTAAGATGAACACAGAAAGGGCAAAGGTCAGTGAAGTCTAGGCTCTCTATCCC T C RF00017-1784 RNACentral:URS0000904F64 SRP RNA intron GSE85324:GSM2264767,GSM2264768,GSM2264769,GSM2264770,GSE87190:GSM2324296,GSM2324295,GSE97408:GSM2564019,GSM2564017,GSE120229:GSM3396437,GSM3396438,GSM3396441,GSM3396442 hESCs,H1 Ribominus eluate replicate 1;peripheral blood, shNS-PBS,tumor: acute monocytic leukemia, treatment: shNS-PBS;acute myeloid leukemia (AML),NB4?shNS (non-specific control);HEK293T,wild type chr6:33403476..33406920,chr6:33400488..33406232,chr6:33400488..33406300,chr6:33403476..33404150 28854373,29249359,29290617 MeRIP-seq:(Medium) rs1434919835 Functional Loss SNV dbSNP153 33..33 33 - - - 6_33403708 chr6:33403708 T C 1.2 1.8e-19 1.25-1.15 0.182321556793955 0.0202022496915529 9.0248145418274 364331 RMVar_ID_364331 Human_SNP_ID_272469349 m6A Human - 33403708 33403708 GAACACCTGATGCTAAGATGAACACAGAAAGGACAAAGGTCAGTGAAGTCTAGGCTCTCTATCCC GAACACCTGATGCTAAGATGAACACAGAAAGGTCAAAGGTCAGTGAAGTCTAGGCTCTCTATCCC T A RF00017-1784 RNACentral:URS0000904F64 SRP RNA intron GSE85324:GSM2264767,GSM2264768,GSM2264769,GSM2264770,GSE87190:GSM2324296,GSM2324295,GSE97408:GSM2564019,GSM2564017,GSE120229:GSM3396437,GSM3396438,GSM3396441,GSM3396442 hESCs,H1 Ribominus eluate replicate 1;peripheral blood, shNS-PBS,tumor: acute monocytic leukemia, treatment: shNS-PBS;acute myeloid leukemia (AML),NB4?shNS (non-specific control);HEK293T,wild type chr6:33403476..33406920,chr6:33400488..33406232,chr6:33400488..33406300,chr6:33403476..33404150 28854373,29249359,29290617 MeRIP-seq:(Medium) rs1434919835 Functional Loss SNV dbSNP153 33..33 33 - - -