| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs15150 | snp | C/G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-3-prime | NOP2, CHD4 | GRCh38.p7 | 12:6570302 | TTTATTTTGTGTTTT[C/G/T]TTTTCTCCTTTTTGG | 1108 |
| rs1057510 | snp | A/G | 0.448708 | 0.151707 | intron-variant | CHD4 | GRCh38.p7 | 12:6574121 | AGCAACTTTTCTAAT[A/G]TAGTAATACTGTGGC | 1108 |
| rs1639122 | snp | A/C | 0.484446 | 0.0868443 | missense | CHD4 | GRCh38.p7 | 12:6601981 | ATCATCATCATCATC[A/C]TCCTCCTCCTCCTCC | 1108 |
| rs1639123 | snp | C/T | 0.449853 | 0.150196 | intron-variant | CHD4 | GRCh38.p7 | 12:6605502 | AAAACACAGATAGCG[C/T]AACCCCTAGCACACC | 1108 |
| rs1734114 | snp | A/G | 0.437683 | 0.165152 | intron-variant | CHD4 | GRCh38.p7 | 12:6604284 | ATCTCAAAAATAAAA[A/G]AGAAAATAATATCCC | 1108 |
| rs1734115 | snp | C/G | 0.0448719 | 0.142907 | intron-variant | CHD4 | GRCh38.p7 | 12:6605873 | CAGCAACCACAGGAT[C/G]CTACTAGCACAGATG | 1108 |
| rs1734116 | snp | A/G | 0.434831 | 0.168337 | utr-variant-5-prime | CHD4 | GRCh38.p7 | 12:6606427 | CCTGCCGGCGGCCTG[A/G]GGACCTCTACACTGG | 1108 |
| rs2267968 | snp | A/G | 0.148996 | 0.228688 | utr-variant-3-prime | CHD4 | GRCh38.p7 | 12:6570577 | GGAAGATGGGCAGAA[A/G]GAAGGTGAGGGTCTC | 1108 |
| rs2267969 | snp | A/C | 0.251887 | 0.249993 | intron-variant, downstream-variant-500B | CHD4, SCARNA11 | GRCh38.p7 | 12:6581020 | AAACAAACAAACAAA[A/C]AAAAAAAATGTGGAT | 1108 |
| rs2267970 | snp | A/G | 0.150333 | 0.229274 | intron-variant, upstream-variant-2KB | CHD4, SCARNA11 | GRCh38.p7 | 12:6582393 | TGGCTCCACCTTGAG[A/G]TAAAGCCCACCACTG | 1108 |
| rs2267971 | snp | C/T | 0.0418186 | 0.138422 | intron-variant | CHD4 | GRCh38.p7 | 12:6600150 | TTTCCATCCAGGCCC[C/T]GAAGAGCTTTACTGT | 1108 |
| rs2267972 | snp | A/G | 0.0558544 | 0.157504 | intron-variant | CHD4 | GRCh38.p7 | 12:6604925 | ACTACTGTTTCTCAT[A/G]CCCCTCTCAGAAGGA | 1108 |
| rs2267973 | snp | A/G | 0.164219 | 0.234823 | intron-variant | CHD4 | GRCh38.p7 | 12:6604940 | GCCCCTCTCAGAAGG[A/G]CAGGGTCCCCTTACC | 1108 |
| rs2267974 | snp | A/G | 0.0905955 | 0.192588 | synonymous-codon | CHD4 | GRCh38.p7 | 12:6606361 | GGGACGGGGAGCCCA[A/G]GCCCGACGCCATCCC | 1108 |
| rs2284324 | snp | A/T | 0 | 0 | intron-variant | CHD4 | GRCh38.p7 | 12:6579230 | CAAGGTGGGTGGATC[A/T]CCTGAGGTGAGGAGT | 1108 |
| rs2284325 | snp | A/T | 0.423726 | 0.179776 | intron-variant | CHD4 | GRCh38.p7 | 12:6595047 | ATTAAGCCAGATTCC[A/T]ATGTAAGTGCATAAA | 1108 |
| rs3831756 | in-del | -/A | | | intron-variant, downstream-variant-500B | CHD4, SCARNA11 | GRCh38.p7 | 12:6581019 | aaacaaacaaacaaa[-/A]caaAAAAAATGTGGA | 1108 |
| rs3834496 | in-del | -/C | | | upstream-variant-2KB | CHD4 | GRCh38.p7 | 12:6608045 | ATAGTCAGAAACTCA[-/C]CCCCCCCCATACTAC | 1108 |
| rs4764608 | snp | A/G | 0.0614824 | 0.164198 | intron-variant | CHD4 | GRCh38.p7 | 12:6596998 | aaataggccgagtgc[A/G]gcggctcacgcctgt | 1108 |
| rs5796243 | in-del | -/G | | | intron-variant | CHD4 | GRCh38.p7 | 12:6573460 | TTTCCCTTTTTCAAT[-/G]TCCTCATTTTTAAAA | 1108 |
| rs6489723 | snp | C/G/T | 0.276123 | 0.248631 | intron-variant | CHD4 | GRCh38.p7 | 12:6574654 | TTCTGATCCCACTAG[C/G/T]GTATGGTGATGGGGG | 1108 |
| rs7132970 | snp | C/T | 0.228105 | 0.249039 | intron-variant | CHD4 | GRCh38.p7 | 12:6599732 | ACATAGAAAAGACTA[C/T]ACTTTCCCATTTTTT | 1108 |
| rs7294416 | snp | A/T | 0.212122 | 0.247114 | intron-variant | CHD4 | GRCh38.p7 | 12:6580520 | gagactggcctgacc[A/T]atatggagaaacccc | 1108 |
| rs7303171 | snp | C/T | 0.330016 | 0.236849 | intron-variant | CHD4 | GRCh38.p7 | 12:6576439 | ctcattgcagcctcc[C/T]aagtagctggaacta | 1108 |
| rs7303399 | snp | A/T | 0.131381 | 0.220067 | intron-variant | CHD4 | GRCh38.p7 | 12:6599647 | CAACACTATAGGATG[A/T]AGGAGAATACCTTTC | 1108 |
| rs7305251 | snp | A/G | 0.423726 | 0.179776 | intron-variant | CHD4 | GRCh38.p7 | 12:6597315 | TAAAGATAATAACAT[A/G]AAGTgtcaggcgcag | 1108 |
| rs7305490 | snp | C/T | 0.0418186 | 0.138422 | intron-variant | CHD4 | GRCh38.p7 | 12:6596778 | gcactccagcctggg[C/T]gacagaacgagactc | 1108 |
| rs7307709 | snp | A/G | 0.329783 | 0.236927 | intron-variant | CHD4 | GRCh38.p7 | 12:6580043 | cctgggcgacaaagc[A/G]agactccgtctcaaa | 1108 |
| rs7308584 | snp | A/G | 0.426354 | 0.177198 | intron-variant | CHD4 | GRCh38.p7 | 12:6597578 | agaccagcctggcca[A/G]cagaatgaaaaccct | 1108 |
| rs7309207 | snp | A/C | 0.212122 | 0.247114 | intron-variant | CHD4 | GRCh38.p7 | 12:6580519 | ggagactggcctgac[A/C]aatatggagaaaccc | 1108 |
| rs7310535 | snp | C/G/T | 0.0151661 | 0.0857571 | intron-variant | CHD4 | GRCh38.p7 | 12:6598463 | AATCTCAAATCATAA[C/G/T]CATGGGAGGAGAAGG | 1108 |
| rs7311397 | snp | A/G | 0.329084 | 0.237162 | intron-variant | CHD4 | GRCh38.p7 | 12:6580639 | ttgaactcaggaggc[A/G]gaggttgcagtaagc | 1108 |
| rs7316626 | snp | A/G | 0.277213 | 0.248515 | intron-variant, upstream-variant-2KB | CHD4, SCARNA11 | GRCh38.p7 | 12:6582286 | AGACATATGCCCTGT[A/G]TAAAGAAGTAGAGAA | 1108 |
| rs7487055 | snp | A/G | | | intron-variant | CHD4 | GRCh38.p7 | 12:6586027 | attgcttgaacccag[A/G]aagtggaggttgcag | 1108 |
| rs7965883 | snp | A/G | 0.424503 | 0.179021 | intron-variant | CHD4 | GRCh38.p7 | 12:6586621 | tcactcttcagccca[A/G]gagtttaaggttgca | 1108 |
| rs7969177 | snp | A/G | 0.248471 | 0.249995 | intron-variant | CHD4 | GRCh38.p7 | 12:6603814 | GGACTTGTGGTCAGC[A/G]CATACAACCTTCTCC | 1108 |
| rs7973027 | snp | A/C | 0.3744 | 0.216852 | intron-variant | CHD4 | GRCh38.p7 | 12:6579807 | cacgcctgtaatccc[A/C]gcactttgggaggcc | 1108 |
| rs7974020 | snp | A/G | 0.424348 | 0.179172 | intron-variant | CHD4 | GRCh38.p7 | 12:6588676 | ccagctactcaggag[A/G]ctgaggcaggagaac | 1108 |
| rs9630275 | snp | C/T | 0 | 0 | intron-variant | CHD4 | GRCh38.p7 | 12:6592108 | AGAGCCTTTCAATGA[C/T]TAATAATGCAGTGCC | 1108 |
| rs9888313 | snp | A/G | 0.430136 | 0.173352 | intron-variant | CHD4 | GRCh38.p7 | 12:6573845 | CCTGGCCAACATGAC[A/G]AAACCCCGTCTCTAC | 1108 |
| rs10437832 | snp | A/G | 0.115088 | 0.210473 | intron-variant, upstream-variant-2KB | CHD4, SCARNA11 | GRCh38.p7 | 12:6581984 | atttttgtattttta[A/G]tagagatggggtttc | 1108 |
| rs10774438 | snp | C/T | 0.423881 | 0.179625 | intron-variant | CHD4 | GRCh38.p7 | 12:6590699 | AGTGGATCAAGCCTA[C/T]AGCCCCAGCTAGTTG | 1108 |
| rs10849491 | snp | A/C | | | intron-variant | CHD4 | GRCh38.p7 | 12:6591143 | AAAAAAAAAAAAAAA[A/C]AAAAAAAACCTAGTA | 1108 |
| rs11064256 | snp | C/T | 0.0509478 | 0.151255 | intron-variant | CHD4 | GRCh38.p7 | 12:6571372 | CCTTATTTCACCCTC[C/T]GCCTCCTCATAACCT | 1108 |
| rs11064258 | snp | A/G | | | intron-variant | CHD4 | GRCh38.p7 | 12:6572397 | CACCACTGCACTCCA[A/G]CCTGGGCAACAGAGC | 1108 |
| rs11064259 | snp | C/T | 0.115788 | 0.21092 | intron-variant | CHD4 | GRCh38.p7 | 12:6575957 | TTCTACCAAAAAAAT[C/T]TCCGTCGCATTCTTC | 1108 |
| rs11064260 | snp | A/T | 0.418974 | 0.184249 | intron-variant | CHD4 | GRCh38.p7 | 12:6576103 | gtggctcacgcctgt[A/T]atctcagcactttgg | 1108 |
| rs11064261 | snp | A/G | | | intron-variant | CHD4 | GRCh38.p7 | 12:6580122 | AATCCCAGCTACTCA[A/G]AGGCTGAGGCAGGAG | 1108 |
| rs11064262 | snp | A/C | 0.362313 | 0.223351 | intron-variant | CHD4 | GRCh38.p7 | 12:6580232 | ACTCCATCTCGAAAA[A/C]AACAACAACAACAAC | 1108 |
| rs11064263 | snp | A/C | 0 | 0 | intron-variant | CHD4 | GRCh38.p7 | 12:6585015 | AAATCACAGGTAAGC[A/C]TCAGGGAAACACAGC | 1108 |
| rs11064264 | snp | A/C | 0 | 0 | intron-variant | CHD4 | GRCh38.p7 | 12:6585026 | AAGCATCAGGGAAAC[A/C]CAGCAAGGGGGATGG | 1108 |
| rs11064265 | snp | A/C | 0.141934 | 0.225437 | intron-variant | CHD4 | GRCh38.p7 | 12:6585138 | ACAGAGGACAAGAAA[A/C]AGGAAATTTTATTTT | 1108 |
| rs11064266 | snp | A/G | 0.335559 | 0.234904 | intron-variant | CHD4 | GRCh38.p7 | 12:6585489 | GGGTTTCATCGTGTT[A/G]GCCAGGATGGGCTCG | 1108 |
| rs11064267 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | CHD4 | GRCh38.p7 | 12:6585967 | TAGCCGGGCATGGTG[A/G]TGCATACCTGTAATC | 1108 |
| rs11064268 | snp | C/T | 0.424659 | 0.17887 | intron-variant | CHD4 | GRCh38.p7 | 12:6586112 | ATCAAAAAAAAAATA[C/T]ATAAGGCCAGGGGCA | 1108 |
| rs11064269 | snp | A/G | | | intron-variant | CHD4 | GRCh38.p7 | 12:6586816 | AATTCTCCTGCCTCA[A/G]CCTCCCGAACACCTG | 1108 |
| rs11064270 | snp | C/T | 0.148996 | 0.228688 | intron-variant | CHD4 | GRCh38.p7 | 12:6586822 | CCTGCCTCAGCCTCC[C/T]GAACACCTGGGACTA | 1108 |
| rs11064271 | snp | A/G | 0.115788 | 0.21092 | intron-variant | CHD4 | GRCh38.p7 | 12:6590488 | gcaacttttttctaa[A/G]tctaaaattaaaata | 1108 |
| rs11064272 | snp | A/G | 0.332337 | 0.236052 | intron-variant | CHD4 | GRCh38.p7 | 12:6590980 | ATACAAAAATTAGCT[A/G]GGCGTGGTGGCACAC | 1108 |
| rs11064273 | snp | A/C | 0.0452528 | 0.143452 | intron-variant | CHD4 | GRCh38.p7 | 12:6594381 | TTTTTTTATTCCCTT[A/C]TCTCTCTACTCAGTG | 1108 |
| rs11064274 | snp | C/T | | | intron-variant | CHD4 | GRCh38.p7 | 12:6595670 | gcagacgcctgtaat[C/T]tcagctactcgggag | 1108 |
| rs11064275 | snp | G/T | 0.226188 | 0.248863 | intron-variant | CHD4 | GRCh38.p7 | 12:6596771 | CGCCACTGCACTCCA[G/T]CCTGGGCGACAGAAC | 1108 |
| rs11064276 | snp | A/G | 0.162581 | 0.234218 | intron-variant | CHD4 | GRCh38.p7 | 12:6597816 | CAAGTCTAAGTTACT[A/G]GTGACAGCCATTTTC | 1108 |
| rs11064278 | snp | C/G/T | 1.64749e-05 | 0.00287005 | intron-variant | CHD4 | GRCh38.p7 | 12:6602336 | TCAGAGCTCCTCCCT[C/G/T]CTTCCTCTGATTCCC | 1108 |
| rs11064279 | snp | C/T | | | intron-variant | CHD4 | GRCh38.p7 | 12:6603776 | TTTCAATCATCAGAG[C/T]TGAGATTTAACAAAG | 1108 |
| rs11064280 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CHD4 | GRCh38.p7 | 12:6604900 | GTGGAACCCAGAATG[C/T]TTAGGCAGCACTACT | 1108 |
| rs11539542 | snp | C/T | 0.224741 | 0.248721 | synonymous-codon | CHD4 | GRCh38.p7 | 12:6599893 | GGAATTCTGTCGGGT[C/T]TGCAAGGATGGTGGG | 1108 |
| rs11539543 | snp | C/T | 0.225314 | 0.248778 | synonymous-codon | CHD4 | GRCh38.p7 | 12:6598360 | TCAGCCACCATCTCC[C/T]ACACCAGTGCCTCGG | 1108 |
| rs11830845 | snp | C/G | 0 | 0 | upstream-variant-2KB | CHD4 | GRCh38.p7 | 12:6607598 | GCCCCCTTCGCAGCG[C/G]GCGCGCGCGCGTCAC | 1108 |
| rs11833125 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | CHD4 | GRCh38.p7 | 12:6576220 | aaattagctgggcgt[A/G]gtggcacacgcctgt | 1108 |
| rs11833796 | snp | C/T | 0.340108 | 0.233197 | intron-variant | CHD4 | GRCh38.p7 | 12:6590381 | taccaatgttaattt[C/T]ctagttttgatcatt | 1108 |
| rs11834945 | snp | A/G | 0.162581 | 0.234218 | intron-variant | CHD4 | GRCh38.p7 | 12:6584547 | TGAGCAACCACACTC[A/G]GCTAATGTTTTTATT | 1108 |
| rs12099908 | snp | A/C | 0.336245 | 0.234652 | intron-variant | CHD4 | GRCh38.p7 | 12:6604470 | GACCAGGCACAAGAA[A/C]GCCCCTCCCATTCCC | 1108 |
| rs12301764 | snp | A/G | 0.0479149 | 0.147179 | upstream-variant-2KB | CHD4 | GRCh38.p7 | 12:6608544 | CCCCCATCTCCAGGC[A/G]CTGTCAGTCTATTCT | 1108 |
| rs12310569 | snp | A/G | 0.227074 | 0.248947 | intron-variant | CHD4 | GRCh38.p7 | 12:6588187 | ACACAAAAAGAATCT[A/G]TTGTTTCTCACTTAA | 1108 |
| rs12312677 | snp | A/G | 0.0475351 | 0.146656 | intron-variant | CHD4 | GRCh38.p7 | 12:6589507 | ggcgtggtggctcac[A/G]cctgtaatcccagca | 1108 |
| rs12315480 | snp | C/G | 0.0479149 | 0.147179 | upstream-variant-2KB | CHD4 | GRCh38.p7 | 12:6608265 | TATCAAAAAGATAAC[C/G]CATAATGATCAACAG | 1108 |
| rs12321714 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | CHD4 | GRCh38.p7 | 12:6576096 | gggcacagtggctca[C/T]gcctgttatctcagc | 1108 |
| rs12322604 | snp | A/G | 0.334182 | 0.235401 | upstream-variant-2KB | CHD4 | GRCh38.p7 | 12:6608479 | CATCTCCACTCTACC[A/G]CCCCTATACCCTTCG | 1108 |
| rs12812446 | snp | C/T | | | intron-variant | CHD4 | GRCh38.p7 | 12:6600436 | GTTATTGGAAAAAAA[C/T]TACCTCCCCCCACCC | 1108 |
| rs12813188 | snp | A/C | | | intron-variant | CHD4 | GRCh38.p7 | 12:6600435 | AGTTATTGGAAAAAA[A/C]CTACCTCCCCCCACC | 1108 |
| rs12813401 | snp | A/G | | | intron-variant | CHD4 | GRCh38.p7 | 12:6586121 | aaaaTATATAAggcc[A/G]ggggcagtggctcac | 1108 |
| rs12816349 | snp | A/G | 0.297128 | 0.245518 | intron-variant | CHD4 | GRCh38.p7 | 12:6600779 | ATCCCAGCAAGCACC[A/G]TTATACAGGGAGCCT | 1108 |
| rs12818623 | snp | C/T | | | intron-variant | CHD4 | GRCh38.p7 | 12:6601194 | TCCTCCCTCCTATCT[C/T]CTACCTTAGGGCTGA | 1108 |
| rs12818651 | snp | C/T | 1.67402e-05 | 0.00289306 | intron-variant | CHD4 | GRCh38.p7 | 12:6601241 | TGCTGTCTTTGACAT[C/T]TTAAGCCCACACTAG | 1108 |
| rs12824453 | snp | G/T | | | intron-variant | CHD4 | GRCh38.p7 | 12:6601231 | AGCATTCCCATGCTG[G/T]CTTTGACATCTTAAG | 1108 |
| rs16927894 | in-del | -/GAA | | | upstream-variant-2KB | CHD4 | GRCh38.p7 | 12:6607849 | ATTAGGTCCAAGAGT[-/GAA]GAAGAAGTTGGCAAA | 1108 |
| rs16928087 | snp | G/T | | | upstream-variant-2KB | CHD4 | GRCh38.p7 | 12:6607894 | GCCATGGGGAGGGAG[G/T]GGTGATGAATTATTA | 1108 |
| rs16932768 | snp | C/T | 0.00743484 | 0.0605156 | missense | CHD4 | GRCh38.p7 | 12:6578864 | TGTCTTCTACCACAA[C/T]AGGGGTCAGATCTAT | 1108 |
| rs17726105 | snp | A/G | 1.6588e-05 | 0.00287988 | intron-variant, upstream-variant-2KB | CHD4, SCARNA11 | GRCh38.p7 | 12:6582761 | TACCTAGGGGAAGAA[A/G]AAACCCAGGTGAGAG | 1108 |
| rs17788043 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant, upstream-variant-2KB | CHD4, SCARNA11 | GRCh38.p7 | 12:6583506 | TACTTGGTGTGCCTG[C/T]TTGGACCTAAGAACT | 1108 |
| rs17788055 | snp | A/T | 0.0283406 | 0.115616 | intron-variant | CHD4 | GRCh38.p7 | 12:6583846 | ACTGTCTGCAGAACG[A/T]AAAGAATTCTATATA | 1108 |
| rs17790300 | snp | A/G | 0.148996 | 0.228688 | intron-variant | CHD4 | GRCh38.p7 | 12:6576022 | CCATTTGTGAGTTCC[A/G]TCCCTACTCCAATTC | 1108 |
| rs28866502 | snp | C/T | 0.448323 | 0.15221 | intron-variant | CHD4 | GRCh38.p7 | 12:6572043 | AGGCAGGAGAATCAC[C/T]TGAACACAGGAGGCG | 1108 |
| rs34219949 | in-del | -/T | 0.0244538 | 0.107838 | upstream-variant-2KB | CHD4 | GRCh38.p7 | 12:6608484 | CCACTCTACCACCCC[-/T]ATACCCTTCGAGCCA | 1108 |
| rs34224003 | in-del | -/A | | | intron-variant, upstream-variant-2KB | CHD4, SCARNA11 | GRCh38.p7 | 12:6582951 | GCTGCAAGAAGAAAA[-/A]GATGAATGAGTGACA | 1108 |
| rs34260297 | in-del | -/A | | | upstream-variant-2KB | CHD4 | GRCh38.p7 | 12:6609011 | TGGGGATGGACATCC[-/A]CATCACGATGTGAAC | 1108 |
| rs34287606 | in-del | -/C | | | upstream-variant-2KB | CHD4 | GRCh38.p7 | 12:6609134 | CCTAGCAAGGCCGAG[-/C]TCCGCACCATGGAGA | 1108 |
| rs34509399 | snp | C/T | 0.00267675 | 0.0364858 | synonymous-codon | CHD4 | GRCh38.p7 | 12:6578040 | CTACTGGCTGCTAGC[C/T]GGCATTATAAAGTAT | 1108 |
| rs34659145 | in-del | -/G | | | intron-variant | CHD4 | GRCh38.p7 | 12:6595199 | TGTGGAGAAGTGGGG[-/G]AAGCCGACTTTGTGA | 1108 |
| rs34714666 | snp | A/C | | | intron-variant | CHD4 | GRCh38.p7 | 12:6597277 | CTGTCTCAAAAAAAA[A/C]CAATAATAATAAAAT | 1108 |
| rs34720286 | in-del | -/T | | | intron-variant | CHD4 | GRCh38.p7 | 12:6605195 | AGAAGGCAGAAGTGA[-/T]ATGATGCTGGATGAG | 1108 |
| rs34863790 | snp | A/G | 0.0468802 | 0.145748 | synonymous-codon, upstream-variant-2KB | CHD4, SCARNA11 | GRCh38.p7 | 12:6581743 | GGAGGAAAACAAGAA[A/G]ATGTCCCAGCCAGGG | 1108 |
| rs34889698 | in-del | -/C | | | intron-variant | CHD4 | GRCh38.p7 | 12:6574235 | GCTTTTTCTTCTCCC[-/C]ACTACATACCTTTTA | 1108 |
| rs35011913 | in-del | -/A | 0 | 0 | intron-variant | CHD4 | GRCh38.p7 | 12:6591151 | AAAAAAAAAAAAAAA[-/A]CCTAGTAGCGTCTAC | 1108 |
| rs35105693 | in-del | -/C | | | intron-variant | CHD4 | GRCh38.p7 | 12:6571170 | TCTGACCTGACCTCC[-/C]ACCATGTTCAAATTC | 1108 |
| rs35512811 | snp | C/T | 0.013172 | 0.080078 | missense | CHD4 | GRCh38.p7 | 12:6578884 | AGGTGGAGGAAAAGT[C/T]AGCAATAGATCTGAC | 1108 |
| rs35536354 | in-del | -/A | | | intron-variant | CHD4 | GRCh38.p7 | 12:6570859 | GTGTCAAGAAGAAAA[-/A]TGGTCCTACCTGCTG | 1108 |
| rs35630388 | in-del | -/T | | | intron-variant | CHD4 | GRCh38.p7 | 12:6576063 | ACTTTTTTTTTTTTT[-/T]AAGACAGGGTCTTGG | 1108 |
| rs36045653 | snp | C/T | 0.163564 | 0.234582 | intron-variant | CHD4 | GRCh38.p7 | 12:6572502 | TCAGGAGGCTGAGGC[C/T]GGAGGATCACTTGAA | 1108 |
| rs55670476 | snp | A/C | 0.238364 | 0.249729 | intron-variant, downstream-variant-500B | CHD4, SCARNA11 | GRCh38.p7 | 12:6581024 | AAACAAACAAACAAA[A/C]AAAATGTGGATACCT | 1108 |
| rs57158128 | in-del | -/A | | | intron-variant | CHD4 | GRCh38.p7 | 12:6579602 | CAAAAAAAAAAAAAA[-/A]CAACAACAAAAAAAA | 1108 |
| rs57266458 | in-del | -/A/AAAA | | | intron-variant | CHD4 | GRCh38.p7 | 12:6580727 | AAAAAAAAAAAAAAA[-/A/AAAA]GCCAGGCACAGTGGC | 1108 |
| rs57833153 | snp | A/G | | | intron-variant | CHD4 | GRCh38.p7 | 12:6604608 | CACCACCCCCATAAA[A/G]GCTGGAAGTGGAGAC | 1108 |
| rs58925722 | in-del | -/A | | | intron-variant | CHD4 | GRCh38.p7 | 12:6590212 | GAAGAAGAAAAAAAA[-/A]TCTGTATCATATAAG | 1108 |
| rs59172392 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | CHD4 | GRCh38.p7 | 12:6572082 | AGTGAGCCGAGATCA[C/T]GCCATTGCACCCCAG | 1108 |
| rs60122715 | in-del | -/G | | | intron-variant | CHD4 | GRCh38.p7 | 12:6571732 | TGGGAGGCAGAGGCG[-/G]GTGGATCACCTGAGA | 1108 |
| rs60218832 | in-del | -/AA | 0.32955 | 0.237006 | intron-variant | CHD4 | GRCh38.p7 | 12:6573917 | TAACTGCAGCTACTC[-/AA]GAGGTTGAGGCAGAA | 1108 |
| rs60576712 | snp | C/T | | | intron-variant | CHD4 | GRCh38.p7 | 12:6579232 | AGGTGGGTGGATCAC[C/T]TGAGGTGAGGAGTTA | 1108 |
| rs60612268 | snp | A/G | | | intron-variant | CHD4 | GRCh38.p7 | 12:6579157 | CAATCTCTATTAAAA[A/G]TACAAAAATTAGCTG | 1108 |
| rs60669376 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | CHD4 | GRCh38.p7 | 12:6590131 | TGAACCCAGGAGGCA[C/T]AGGTTGCAATGAGTC | 1108 |
| rs60782986 | snp | C/T | | | intron-variant | CHD4 | GRCh38.p7 | 12:6579151 | GAACCCCAATCTCTA[C/T]TAAAAATACAAAAAT | 1108 |
| rs60910415 | in-del | -/AA | | | intron-variant | CHD4 | GRCh38.p7 | 12:6577438 | AAAAAAAAAAAAAAA[-/AA]CAACCAGCAGCCCAC | 1108 |
| rs61518872 | in-del | -/A | | | intron-variant | CHD4 | GRCh38.p7 | 12:6579770 | AAAAAAAAAAAAAAA[-/A]TTTTGGCCAGGCGTG | 1108 |
| rs61697243 | in-del | -/A | | | intron-variant | CHD4 | GRCh38.p7 | 12:6577439 | AAAAAAAAAAAAAAA[-/A]CAACCAGCAGCCCAC | 1108 |
| rs61753200 | snp | C/T | 0.0261329 | 0.111281 | synonymous-codon | CHD4 | GRCh38.p7 | 12:6597938 | CCACTCGGGTTTTAT[C/T]CCATAGCGATAGAAG | 1108 |
| rs61753201 | snp | C/T | 0.031737 | 0.121908 | intron-variant | CHD4 | GRCh38.p7 | 12:6601957 | GGATGGAGGTCCAGG[C/T]ACCTTTGAATCATCA | 1108 |
| rs61759470 | snp | A/G | 0.00123698 | 0.0248387 | synonymous-codon | CHD4 | GRCh38.p7 | 12:6593133 | GGCTTCATCCACGAT[A/G]AGGCAGGCCCAATCA | 1108 |
| rs61759471 | snp | C/T | 0.0132582 | 0.0803325 | intron-variant | CHD4 | GRCh38.p7 | 12:6598219 | AGACTATCCTAAACT[C/T]ACCTGCAGTTCAGAA | 1108 |
| rs61918041 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | CHD4 | GRCh38.p7 | 12:6572702 | AGCTAGGATTATAAG[C/T]GTGCGTTGCGCCACA | 1108 |
| rs61918042 | snp | A/T | 0 | 0 | intron-variant | CHD4 | GRCh38.p7 | 12:6580079 | AAAAAAAAAAAAAAT[A/T]ACGTGGGCATGGTTG | 1108 |
| rs61918043 | snp | G/T | | | intron-variant | CHD4 | GRCh38.p7 | 12:6587365 | ACCAAGCACAGGATT[G/T]CCTTGGATTCATACT | 1108 |
| rs61918044 | snp | A/G | | | intron-variant | CHD4 | GRCh38.p7 | 12:6590059 | CAAAAATCTGGGCCC[A/G]TGGTGGCACACACCC | 1108 |
| rs61918045 | snp | A/T | 0.5 | 0 | intron-variant | CHD4 | GRCh38.p7 | 12:6596505 | AAAAAAAAAAAAAAT[A/T]AGCCAGGCATCAGGC | 1108 |
| rs66627071 | snp | C/T | 0.209997 | 0.246779 | intron-variant | CHD4 | GRCh38.p7 | 12:6596214 | AAAAACTGGCAATAC[C/T]GTTTGTTTCACACCA | 1108 |
| rs67013744 | snp | A/G | 0.345925 | 0.230864 | intron-variant | CHD4 | GRCh38.p7 | 12:6572620 | CCTGTGCAATGGCAC[A/G]ATCTTGGCTCACTGC | 1108 |
| rs71445111 | snp | G/T | 0.5 | 0 | intron-variant | CHD4 | GRCh38.p7 | 12:6571769 | GTTCAAGACCAGCCT[G/T]GCCAACATGGTGAAA | 1108 |
| rs71445112 | snp | C/T | 0.5 | 0 | intron-variant | CHD4 | GRCh38.p7 | 12:6571786 | CCAACATGGTGAAAC[C/T]CCATCTCTACTAAAA | 1108 |
| rs71445113 | snp | C/T | 0.5 | 0 | intron-variant | CHD4 | GRCh38.p7 | 12:6571875 | CTGAGGCAGGAGAAT[C/T]GCTTGAACCCGGGAG | 1108 |
| rs71445114 | snp | A/G | 0.5 | 0 | intron-variant | CHD4 | GRCh38.p7 | 12:6572351 | GAATCGCTTGAACCC[A/G]GGAGGCGGAGATTGT | 1108 |
| rs71445115 | snp | A/G | 0.5 | 0 | intron-variant | CHD4 | GRCh38.p7 | 12:6572358 | TTGAACCCGGGAGGC[A/G]GAGATTGTGGTGGGC | 1108 |
| rs71445116 | snp | A/G | 0.5 | 0 | intron-variant | CHD4 | GRCh38.p7 | 12:6572362 | ACCCGGGAGGCGGAG[A/G]TTGTGGTGGGCCAAG | 1108 |
| rs71445117 | snp | C/T | 0.5 | 0 | intron-variant | CHD4 | GRCh38.p7 | 12:6577304 | GCAGGCGCCTGTAAT[C/T]TCAGCTACTCAGGAG | 1108 |
| rs71445118 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | CHD4 | GRCh38.p7 | 12:6584465 | AGTAGAGTGGCGTCA[A/T]TACGGCTCACTGCAG | 1108 |
| rs71445119 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | CHD4 | GRCh38.p7 | 12:6584468 | AGAGTGGCGTCATTA[A/C]GGCTCACTGCAGCCT | 1108 |
| rs71445120 | snp | C/G | 0.231775 | 0.249335 | intron-variant | CHD4 | GRCh38.p7 | 12:6590005 | GGAGTTCGAGACCAG[C/G]CTGGCCAACATGGTG | 1108 |
| rs71450158 | in-del | -/T | 0.5 | 0 | intron-variant | CHD4 | GRCh38.p7 | 12:6571677 | CTAAAAATACAAAAT[-/T]AGCTGGGGCGCAGTG | 1108 |
| rs71450159 | in-del | -/G | 0.5 | 0 | intron-variant | CHD4 | GRCh38.p7 | 12:6595823 | TCAGCTAGGTGTGGT[-/G]GGCGTATGCAAATAA | 1108 |
| rs71459037 | multinucleotide-polymorphism | AGGC/GCAT | 0.5 | 0 | intron-variant | CHD4 | GRCh38.p7 | 12:6571830 | GCTGGGCATGGTGGC[AGGC/GCAT]GCCTGTAATCCCAGC | 1108 |
| rs71579343 | snp | G/T | | | utr-variant-5-prime, upstream-variant-2KB | CHD4 | GRCh38.p7 | 12:6607366 | CGGCTCCTCCTCGCC[G/T]CGGCCGAAGGGGGGA | 1108 |
| rs71579344 | snp | A/C | | | utr-variant-5-prime, upstream-variant-2KB | CHD4 | GRCh38.p7 | 12:6607345 | GGCTCGGTGTCACTC[A/C]CGCTCCGGCTCCTCC | 1108 |
| rs71579345 | snp | A/G | | | intron-variant | CHD4 | GRCh38.p7 | 12:6600526 | AAATATACAGAAGAG[A/G]AACACACCTTTCTTT | 1108 |
| rs71584858 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CHD4 | GRCh38.p7 | 12:6606469 | GTGCGGGGGAGGGGG[A/G]AGAAACACAGAACAG | 1108 |
| rs71584859 | snp | C/G | | | intron-variant, upstream-variant-2KB | CHD4 | GRCh38.p7 | 12:6606465 | CACTGTGCGGGGGAG[C/G]GGGGAGAAACACAGA | 1108 |
| rs71584860 | snp | A/G | 0.00906017 | 0.0666933 | utr-variant-5-prime | CHD4 | GRCh38.p7 | 12:6606400 | CCCGGCCAGGGAATT[A/G]GCCCAGCTGCTCCTG | 1108 |
| rs71584861 | snp | C/G | 0.000832087 | 0.0203802 | utr-variant-5-prime | CHD4 | GRCh38.p7 | 12:6606387 | ATCCCCTTCCGCTCC[C/G]GGCCAGGGAATTGGC | 1108 |
| rs71584862 | snp | C/T | 0.0907993 | 0.192757 | intron-variant | CHD4 | GRCh38.p7 | 12:6606256 | CTTCCCGCCATGGGC[C/T]CTTGGGGAAGATGTT | 1108 |
| rs71584864 | snp | A/G/T | 0.000131789 | 0.00811666 | intron-variant | CHD4 | GRCh38.p7 | 12:6602353 | TTCCTCTGATTCCCC[A/G/T]TAACATTCAGTCACC | 1108 |
| rs71584865 | in-del | -/CCT | | | cds-indel | CHD4 | GRCh38.p7 | 12:6601998 | CCTCCTCCTCCTCCT[-/CCT]TCCGCTTGGATTTGC | 1108 |
| rs71584866 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon | CHD4 | GRCh38.p7 | 12:6587504 | TAGCAGCCGTTCAAT[A/G]GCCTTATCATCGTAG | 1108 |
| rs71584867 | snp | C/T | 0.000164745 | 0.00907442 | synonymous-codon | CHD4 | GRCh38.p7 | 12:6577857 | TTCACCCTTGAAAGG[C/T]TCATTGAGGATGGCA | 1108 |
| rs71584868 | snp | A/G | 0.0105867 | 0.0719812 | synonymous-codon | CHD4 | GRCh38.p7 | 12:6577854 | CATTTCACCCTTGAA[A/G]GGCTCATTGAGGATG | 1108 |
| rs73045994 | snp | C/G | 0.00716266 | 0.059414 | upstream-variant-2KB, utr-variant-3-prime | NOP2, CHD4 | GRCh38.p7 | 12:6570294 | AATACCCCCCAAAAA[C/G]GAGAAAAGAAAACAC | 1108 |
| rs73047807 | snp | C/G | 0.126219 | 0.217206 | intron-variant | CHD4 | GRCh38.p7 | 12:6595003 | TCAAATTACACTGTA[C/G]AAACAAAACCCAGAG | 1108 |
| rs73264831 | snp | A/C | 0.338523 | 0.233803 | intron-variant | CHD4 | GRCh38.p7 | 12:6586419 | ATAAATAAATAAATA[A/C]ATACATACATACATA | 1108 |
| rs73264846 | snp | A/G | 0.212728 | 0.247206 | upstream-variant-2KB | CHD4 | GRCh38.p7 | 12:6608092 | CCTCCTCCCACACAC[A/G]TCCCGTAATAATCAG | 1108 |
| rs74058650 | snp | A/G | 0.152667 | 0.230274 | upstream-variant-2KB, downstream-variant-500B | NOP2, CHD4 | GRCh38.p7 | 12:6569733 | CTCAGCCTTCCTAGA[A/G]ACTAACATTAAGGTA | 1108 |
| rs74058663 | snp | C/T | 0.0414363 | 0.137845 | intron-variant | CHD4 | GRCh38.p7 | 12:6593335 | TACCCTTTTGCCTCA[C/T]CAGGGACCAGATCAC | 1108 |
| rs74364034 | snp | C/G | 0.5 | 0 | intron-variant | CHD4 | GRCh38.p7 | 12:6599251 | AGCCTGGGCAACATA[C/G]TGAGACCCTGTCTCA | 1108 |
| rs74396750 | snp | A/T | 0.5 | 0 | intron-variant | CHD4 | GRCh38.p7 | 12:6599285 | GAGATTTTTTTTTTT[A/T]AATTAGCTGGATGTG | 1108 |
| rs74470219 | snp | A/G | 0.015313 | 0.086151 | intron-variant | CHD4 | GRCh38.p7 | 12:6577758 | AAGTTTGTCACTTAA[A/G]CAATATATTCCTCCC | 1108 |
| rs74506931 | snp | A/C | | | upstream-variant-2KB | CHD4 | GRCh38.p7 | 12:6607715 | ACACACACACACACA[A/C]AACACACACACACCC | 1108 |
| rs74687199 | in-del | -/A | | | intron-variant | CHD4 | GRCh38.p7 | 12:6577266 | AAAATCCAAAAAAAA[-/A]CAGCTGGGTGTGGTG | 1108 |
| rs74790047 | snp | A/C/G | 0.0146672 | 0.084371 | synonymous-codon, missense | CHD4 | GRCh38.p7 | 12:6601978 | TGAATCATCATCATC[A/C/G]TCCTCCTCCTCCTCC | 1108 |
| rs74846136 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6589951 | CACCTGTAATCCCAG[A/C]ACTTTGGGAGGCCAA | 1108 |
| rs74871915 | snp | A/G | 0.0221652 | 0.103281 | intron-variant | CHD4 | GRCh38.p7 | 12:6580377 | CCAGCAAAAATTCAC[A/G]AGTGACCATGGTTCA | 1108 |
| rs74894901 | snp | A/T | 0.5 | 0 | intron-variant | CHD4 | GRCh38.p7 | 12:6598817 | CCATCTCAAAAAAAT[A/T]AAAAAAGATCTCATT | 1108 |
| rs74935314 | snp | A/G | 0.148996 | 0.228688 | intron-variant | CHD4 | GRCh38.p7 | 12:6572697 | TGAGTAGCTAGGATT[A/G]TAAGCGTGCGTTGCG | 1108 |
| rs75789433 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | CHD4, SCARNA11 | GRCh38.p7 | 12:6583013 | AAAAGCAACAAAAAA[A/G]GCACAGCCCTCACCT | 1108 |
| rs75859552 | snp | A/C | | | intron-variant | CHD4 | GRCh38.p7 | 12:6580241 | CGAAAACAACAACAA[A/C]AACAACAACAACAAC | 1108 |
| rs76091967 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | CHD4 | GRCh38.p7 | 12:6605593 | CTAGGAAAAAAGCCA[A/G]AACTATGTCCACTCA | 1108 |
| rs76359472 | snp | C/T | 0.5 | 0 | missense | CHD4 | GRCh38.p7 | 12:6592471 | ACATCGGCTTTGAGC[C/T]GCCGCAACATGTGCG | 1108 |
| rs76527521 | snp | C/T | 0.5 | 0 | missense, upstream-variant-2KB | CHD4, SCARNA11 | GRCh38.p7 | 12:6583227 | GAGCCATCATTGTAG[C/T]TGACCTGTTTACGGA | 1108 |
| rs76548650 | snp | A/C/G | 0.00125522 | 0.0250263 | intron-variant | CHD4 | GRCh38.p7 | 12:6591445 | AGGATTCCTGAAACT[A/C/G]AACAACTCCTTCTCT | 1108 |
| rs76639177 | snp | C/G | 0.0356815 | 0.128715 | intron-variant | CHD4 | GRCh38.p7 | 12:6576633 | TCTTTTTTGAGGTGA[C/G]TCTCGCTCTGTCGCC | 1108 |
| rs77142928 | snp | A/C | 0 | 0 | intron-variant | CHD4 | GRCh38.p7 | 12:6595958 | CAAGACTCCATCTCA[A/C]AAAAAAAAAAAAAGA | 1108 |
| rs77267007 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CHD4 | GRCh38.p7 | 12:6602919 | AGAAGGCAAAAACTA[C/T]AGAATATACCTTCCC | 1108 |
| rs77543056 | snp | C/T | 0.0460142 | 0.144533 | intron-variant | CHD4 | GRCh38.p7 | 12:6587690 | AGCCCCACACCAAAA[C/T]GTAAGTTCCTGACTA | 1108 |
| rs77685609 | snp | C/G | 0 | 0 | intron-variant, upstream-variant-2KB | CHD4 | GRCh38.p7 | 12:6606500 | TCAGTGACGCGCACT[C/G]TCCCCCTCCCCCACA | 1108 |
| rs77843719 | snp | A/G | 0.0722504 | 0.175798 | intron-variant, nc-transcript-variant | CHD4, SCARNA11 | GRCh38.p7 | 12:6581487 | AAATTGTCCTCTCGT[A/G]CCTTTAAGAGCCAGC | 1108 |
| rs77870850 | snp | C/T | 0.5 | 0 | upstream-variant-2KB, utr-variant-3-prime | NOP2, CHD4 | GRCh38.p7 | 12:6570172 | CTTTTTTTTTTTTTC[C/T]ACTTTATTTCATTTA | 1108 |
| rs77877198 | snp | A/G | 0 | 0 | intron-variant | CHD4 | GRCh38.p7 | 12:6572430 | GACTCTATCTCAGAA[A/G]AAAAAAAAAAAAAGA | 1108 |
| rs77900333 | snp | A/C | 0.0205511 | 0.0992634 | intron-variant | CHD4 | GRCh38.p7 | 12:6605505 | ACACAGATAGCGTAA[A/C]CCCTAGCACACCTAC | 1108 |
| rs77921005 | snp | G/T | 0.0115144 | 0.0749975 | upstream-variant-2KB, downstream-variant-500B | NOP2, CHD4 | GRCh38.p7 | 12:6569589 | CCTGGTCTGGGACAT[G/T]AGAAGGGGTGAACTA | 1108 |
| rs77953906 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6583651 | ACAGAATGCTTTCTT[C/G]TAACCCCTTGCACTG | 1108 |
| rs78422207 | snp | A/T | 0 | 0 | intron-variant | CHD4 | GRCh38.p7 | 12:6579774 | AAAAAAAAAAAATTT[A/T]GGCCAGGCGTGGTGG | 1108 |
| rs78428082 | snp | G/T | 0 | 0 | intron-variant | CHD4 | GRCh38.p7 | 12:6576954 | GTCTTTTTTTTTTTT[G/T]GAGACAGAGTCTCAC | 1108 |
| rs78476141 | snp | A/T | 0.5 | 0 | intron-variant | CHD4 | GRCh38.p7 | 12:6580077 | AAAAAAAAAAAAAAA[A/T]TTACGTGGGCATGGT | 1108 |
| rs78577275 | snp | A/C | 0.0402882 | 0.136092 | intron-variant | CHD4 | GRCh38.p7 | 12:6596229 | CGTTTGTTTCACACC[A/C]GACCTCTAGGTATGC | 1108 |
| rs78578768 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | CHD4 | GRCh38.p7 | 12:6606185 | TGCACAGAGACAGCG[A/G]AGCAACACAGCCCTG | 1108 |
| rs78715412 | snp | A/G/T | 1.65466e-05 | 0.00287628 | intron-variant | CHD4 | GRCh38.p7 | 12:6598184 | GTCACTATCCTCTTC[A/G/T]TCGTAGCCCCTACAT | 1108 |
| rs78742502 | snp | C/T | 0.180064 | 0.240019 | intron-variant | CHD4 | GRCh38.p7 | 12:6603593 | CTGCCCTCATAGAAG[C/T]CTCCCCAAATTACCT | 1108 |
| rs78808695 | snp | A/G | 0.14933 | 0.228835 | intron-variant | CHD4 | GRCh38.p7 | 12:6588846 | GCTACTCAGGAAGCT[A/G]AGGCAGGAGAATCAC | 1108 |
| rs78852930 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | CHD4 | GRCh38.p7 | 12:6584186 | GTAGCATTTACATTG[C/G]ATTGGTATTACTTTT | 1108 |
| rs78863562 | snp | C/T | 0.5 | 0 | splice-donor-variant | CHD4 | GRCh38.p7 | 12:6587383 | TTGGATTCATACTCA[C/T]CCCCATTTCTTCTTC | 1108 |
| rs79056447 | snp | C/G | 0.162909 | 0.23434 | intron-variant | CHD4 | GRCh38.p7 | 12:6597046 | AGGAGGAGGTGAGCG[C/G]ATCACAAGGTCAGGC | 1108 |
| rs79063701 | snp | G/T | 0.0275645 | 0.114116 | intron-variant | CHD4 | GRCh38.p7 | 12:6597805 | CCAGTGTCTTCCAAG[G/T]CTAAGTTACTGGTGA | 1108 |
| rs79262687 | snp | A/G | 0.0501905 | 0.150254 | intron-variant | CHD4 | GRCh38.p7 | 12:6574528 | ATATATTCATAAAAC[A/G]TATGACTCAACATAA | 1108 |
| rs79404847 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | CHD4 | GRCh38.p7 | 12:6600481 | CCTTAGGGAGATTCT[A/T]CCCCAATCACTCCCA | 1108 |
| rs79434062 | snp | A/T | 0 | 0 | intron-variant | CHD4 | GRCh38.p7 | 12:6596503 | AAAAAAAAAAAAAAA[A/T]TTAGCCAGGCATCAG | 1108 |
| rs79502086 | snp | C/G | 0.5 | 0 | intron-variant | CHD4 | GRCh38.p7 | 12:6585879 | GAGGCAGGCGGATCA[C/G]TTGAGGTCAGGAGTT | 1108 |
| rs79721088 | snp | A/C | 0.163236 | 0.234461 | intron-variant | CHD4 | GRCh38.p7 | 12:6596964 | ACTCTGTCTCAAAAA[A/C]TATAATAAATAAATA | 1108 |
| rs79722294 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CHD4 | GRCh38.p7 | 12:6573368 | TTGTTTCAGATGGTA[A/G]TAAGAACCTATGAAG | 1108 |
| rs79974709 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | CHD4 | GRCh38.p7 | 12:6598881 | GAGAAAATACAGGTT[A/G]AGGACCCCTCATGTG | 1108 |
| rs80047686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6605470 | ATACGGGTTTGGCCA[A/G]TTCATGAAGCCACCC | 1108 |
| rs111256213 | snp | A/T | 0.5 | 0 | missense | CHD4 | GRCh38.p7 | 12:6600004 | TTCCCACTGGATGCC[A/T]TCCTTCTCCTGCAGT | 1108 |
| rs111351104 | in-del | -/CCC | 0.5 | 0 | upstream-variant-2KB | CHD4 | GRCh38.p7 | 12:6607660 | TAATACACACGGACA[-/CCC]CCCCCCCCAACACAC | 1108 |
| rs111459877 | snp | A/G | 0.5 | 0 | intron-variant | CHD4 | GRCh38.p7 | 12:6593809 | GGTCCCACCATAACT[A/G]CAAGTCTTACCTCTC | 1108 |
| rs111502968 | snp | A/G | | | intron-variant, upstream-variant-2KB | CHD4 | GRCh38.p7 | 12:6607087 | AAGCCGGAGGCGGGG[A/G]GTCGCGGGGAGCAAG | 1108 |
| rs111569582 | snp | C/T | 0.00301028 | 0.0386792 | synonymous-codon | CHD4 | GRCh38.p7 | 12:6601455 | GTTATTGGTACTGAA[C/T]TCCCGCCATTTTGCA | 1108 |
| rs111683971 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CHD4, SCARNA11 | GRCh38.p7 | 12:6582050 | TCAAGTGATCCACCC[A/G]CCTCAGCCTCCCAAA | 1108 |
| rs111755606 | snp | C/T | 0.5 | 0 | intron-variant | CHD4 | GRCh38.p7 | 12:6579042 | AATGTCAGCTGGGCA[C/T]GGTGGCTCATGCCTG | 1108 |
| rs111776336 | snp | A/C | 0.5 | 0 | intron-variant | CHD4 | GRCh38.p7 | 12:6605921 | ACAGAATCCTCAACG[A/C]CCCCCTCCACCACCA | 1108 |
| rs111808702 | snp | A/G | 0.0383715 | 0.133092 | intron-variant | CHD4 | GRCh38.p7 | 12:6580964 | GTAAGCCAAGATCGC[A/G]CCACAGCACTCCAGC | 1108 |
| rs111843039 | snp | C/T | 0.5 | 0 | intron-variant | CHD4 | GRCh38.p7 | 12:6572992 | AAGGAGCTCTGAAAG[C/T]TTGAAAACAAATATA | 1108 |
| rs111980032 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | CHD4 | GRCh38.p7 | 12:6576408 | CCTAGGCTGGAGTGC[A/G]ATGGCACAATCTAGG | 1108 |
| rs112031882 | in-del | -/A | 0.426354 | 0.177198 | intron-variant | CHD4 | GRCh38.p7 | 12:6590204 | TCCATCCCGAAGAAG[-/A]AAAAAAAATCTGTAT | 1108 |
| rs112040841 | snp | G/T | 0.0119091 | 0.0762411 | intron-variant | CHD4 | GRCh38.p7 | 12:6588088 | TTCCTTTTGCACCCC[G/T]GCCTCCAGACACCAC | 1108 |
| rs112065279 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | CHD4 | GRCh38.p7 | 12:6589220 | ATAAAACCTCATTAG[A/G]CAAACACCACAGTAA | 1108 |
| rs112118159 | snp | C/T | 0.5 | 0 | intron-variant | CHD4 | GRCh38.p7 | 12:6594937 | TCAGGATCCACCAGG[C/T]AAATAATCGTTATGT | 1108 |
| rs112122936 | snp | A/T | 0.0107246 | 0.0724382 | intron-variant | CHD4 | GRCh38.p7 | 12:6572539 | AGTTCAAGACCCACC[A/T]GGGCAAAATGGTGAG | 1108 |
| rs112128909 | snp | A/C/G/T | 0.00055444 | 0.016642 | intron-variant, upstream-variant-2KB | CHD4, SCARNA11 | GRCh38.p7 | 12:6582974 | GAGTGACACAGGTAG[A/C/G/T]ATATTAAACAAAGCA | 1108 |
| rs112385586 | snp | A/G | 0.5 | 0 | synonymous-codon | CHD4 | GRCh38.p7 | 12:6600283 | CAGGCAGACCATGTG[A/G]TAAGCACGGGGACAG | 1108 |
| rs112429933 | snp | G/T | | | intron-variant | CHD4 | GRCh38.p7 | 12:6579926 | CCGGGCATGGTGGCA[G/T]GCGCCTGTAGTCCCA | 1108 |
| rs112636750 | snp | A/G/T | 0.000131922 | 0.00812056 | utr-variant-3-prime | CHD4 | GRCh38.p7 | 12:6570660 | TCAGCGGTGGAGGTG[A/G/T]TATCAGTCTGCATCT | 1108 |
| rs112684697 | in-del | -/AA | 0.345037 | 0.231231 | intron-variant | CHD4 | GRCh38.p7 | 12:6585789 | GCAAGACTCTGTCTC[-/AA]AAAAAAAAAAACACA | 1108 |
| rs112688966 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | CHD4 | GRCh38.p7 | 12:6608726 | TTCCAGACACTCGGG[A/G]GCTGGGAGCCCACCT | 1108 |
| rs112763536 | in-del | -/CTT | 0.331874 | 0.236213 | upstream-variant-2KB | CHD4 | GRCh38.p7 | 12:6607842 | GACATCCTTTGCCAA[-/CTT]CTTCTTCACTCTTGG | 1108 |
| rs112798498 | snp | A/T | | | intron-variant | CHD4 | GRCh38.p7 | 12:6596817 | AAAAAAAAATTAGGC[A/T]GGCGTGGTGGCACAC | 1108 |
| rs112803905 | snp | A/G | 1.64757e-05 | 0.00287012 | synonymous-codon | CHD4 | GRCh38.p7 | 12:6593521 | ACCCACATAGGTTAC[A/G]ACATACATGTCTGGA | 1108 |
| rs112876419 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6595604 | ACCAGCCTGGTCAAC[A/G]TGGTGAAACCCCGTC | 1108 |
| rs112882704 | snp | G/T | | | synonymous-codon | CHD4 | GRCh38.p7 | 12:6592467 | GAACACATCGGCTTT[G/T]AGCCGCCGCAACATG | 1108 |
| rs112923427 | snp | A/G | 0.5 | 0 | intron-variant | CHD4 | GRCh38.p7 | 12:6580727 | AAAAAAAAAAAAAAA[A/G]GCCAGGCACAGTGGC | 1108 |
| rs112980730 | snp | A/G | 0.5 | 0 | intron-variant | CHD4 | GRCh38.p7 | 12:6578940 | AAGAAATGTTATTGA[A/G]ACTATACCTAAAGGA | 1108 |
| rs112986829 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | CHD4 | GRCh38.p7 | 12:6590127 | TGCTTGAACCCAGGA[A/G]GCATAGGTTGCAATG | 1108 |
| rs113014142 | snp | A/C | 0.5 | 0 | intron-variant | CHD4 | GRCh38.p7 | 12:6595731 | AGGCGGAGGCTGCAG[A/C]GAGCCAAGATCGCAC | 1108 |
| rs113016182 | snp | C/T | 0.5 | 0 | intron-variant | CHD4 | GRCh38.p7 | 12:6592178 | ACTAAGGACACCTAA[C/T]GCACAAGCACTACCA | 1108 |
| rs113104597 | snp | C/T | 0.216649 | 0.247765 | intron-variant | CHD4 | GRCh38.p7 | 12:6594006 | ACATCCGGCTAATTT[C/T]GTATTTTTAGTAGAG | 1108 |
| rs113168245 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6585210 | TTAAAACAAGCCACA[C/T]ACACATTCCTCACAT | 1108 |
| rs113244573 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | CHD4 | GRCh38.p7 | 12:6575219 | TTGGGAGGACAAGGC[A/G]GGCAGATCACCTGAG | 1108 |
| rs113281544 | snp | A/G | 0.32885 | 0.23724 | intron-variant | CHD4 | GRCh38.p7 | 12:6579351 | GCACTATGGGAGGCC[A/G]AGATGGGTGGATCTC | 1108 |
| rs113366779 | snp | A/G | 0.5 | 0 | intron-variant | CHD4 | GRCh38.p7 | 12:6577502 | TTCAATCCCACCTCT[A/G]TATCTTTCCTGAATA | 1108 |
| rs113378355 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | CHD4 | GRCh38.p7 | 12:6606593 | TGAACTTAGTTCCAC[A/G]CTCCTCGGGGGCAGC | 1108 |
| rs113489387 | snp | C/T | 0.5 | 0 | intron-variant | CHD4 | GRCh38.p7 | 12:6592247 | TAAGTAAGAACTATG[C/T]GCTCCAGCGCCCTAG | 1108 |
| rs113589509 | snp | A/G | 0.5 | 0 | intron-variant | CHD4 | GRCh38.p7 | 12:6577688 | AGAATGAAGAAAGTG[A/G]GAACAGTGCGCTGGA | 1108 |
| rs113606491 | snp | C/T | 0.0295035 | 0.117819 | upstream-variant-2KB | CHD4 | GRCh38.p7 | 12:6607746 | TGCCCCCCCACATTT[C/T]ATACACATATGCCAG | 1108 |
| rs113769285 | snp | A/G | 0.5 | 0 | intron-variant | CHD4 | GRCh38.p7 | 12:6586003 | TACTTGGGAGGCTGA[A/G]GCAGGAGAATTGCTT | 1108 |
| rs113787020 | snp | A/C | 0.5 | 0 | intron-variant | CHD4 | GRCh38.p7 | 12:6588172 | ACAATAAGGTAAACA[A/C]CACAAAAAGAATCTG | 1108 |
| rs113849290 | snp | C/T | 1.67761e-05 | 0.00289617 | intron-variant | CHD4 | GRCh38.p7 | 12:6578555 | TTCTCTTCTACAGAA[C/T]ATGGGGAAGAAAAAT | 1108 |
| rs113879233 | snp | A/C | 9.89038e-05 | 0.00703151 | intron-variant | CHD4 | GRCh38.p7 | 12:6591593 | GGTCATCTGCAAAAG[A/C]AGCACGGTTTAATTA | 1108 |
| rs114035083 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | CHD4 | GRCh38.p7 | 12:6590777 | TGTAGTAAGCCATGA[C/T]TGTGCCACTGCTCTC | 1108 |
| rs114047209 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | CHD4 | GRCh38.p7 | 12:6579546 | CCAAGATCACACCAC[C/T]GCACTGCACATCAGC | 1108 |
| rs114112116 | snp | C/T | 0.00993419 | 0.0697739 | upstream-variant-2KB | CHD4 | GRCh38.p7 | 12:6607815 | ACTAACCCTCTTAGA[C/T]ATCCCATAATAGACA | 1108 |
| rs114120396 | snp | C/T | 0.0448719 | 0.142907 | intron-variant | CHD4 | GRCh38.p7 | 12:6590395 | TTCTAGTTTTGATCA[C/T]TGTACTGCAGTTACG | 1108 |
| rs114435287 | snp | C/T | 0.00144913 | 0.0268787 | intron-variant, upstream-variant-2KB | CHD4, SCARNA11 | GRCh38.p7 | 12:6582318 | GAGTTAAATAGGGAT[C/T]ATGCTGACTCTTAGA | 1108 |
| rs114554098 | snp | A/T | 0.0123036 | 0.0774623 | intron-variant | CHD4 | GRCh38.p7 | 12:6596195 | ACCCTCCTCACTTCC[A/T]CTCAAAAACTGGCAA | 1108 |
| rs114803032 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CHD4 | GRCh38.p7 | 12:6594307 | ATCTACTATCTACTA[A/C]ACACATGTGTACATG | 1108 |
| rs114905614 | snp | A/T | 0.0123036 | 0.0774623 | intron-variant | CHD4 | GRCh38.p7 | 12:6596335 | GAGCTCAAACACCAG[A/T]ATTCAGTCAGTTAAT | 1108 |
| rs115174844 | snp | A/G/T | 0.00263495 | 0.0362022 | synonymous-codon, upstream-variant-2KB | CHD4, SCARNA11 | GRCh38.p7 | 12:6582923 | CAGGCCCTTACGACT[A/G/T]GGCCTACGGGGAGCT | 1108 |
| rs115187275 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | CHD4 | GRCh38.p7 | 12:6587281 | TCATCAACATAAGAA[C/T]TTGCCTACAGATATT | 1108 |
| rs115214161 | snp | A/G | | | intron-variant | CHD4 | GRCh38.p7 | 12:6606014 | ATGCCTGCCAGCCCA[A/G]AGAGCTCCCTCAACT | 1108 |
| rs115239805 | snp | A/T | 0.0123036 | 0.0774623 | intron-variant | CHD4 | GRCh38.p7 | 12:6594940 | GGATCCACCAGGTAA[A/T]TAATCGTTATGTCCC | 1108 |
| rs115252985 | snp | C/G | 9.04593e-05 | 0.00672469 | intron-variant, upstream-variant-2KB | CHD4, SCARNA11 | GRCh38.p7 | 12:6582123 | GAAACAATGGCAAGA[C/G]GCTCAGGGCTCACCT | 1108 |
| rs115269629 | snp | A/G | 0.0148425 | 0.0848584 | intron-variant | CHD4 | GRCh38.p7 | 12:6601271 | GACACCCCCACTCCC[A/G]TTTGAACCCCATTTC | 1108 |
| rs115459539 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | CHD4 | GRCh38.p7 | 12:6604072 | CATTTGAGGTCAGTT[C/T]GAAACCAGCTTGGCC | 1108 |
| rs115587740 | snp | A/G | 0.000529451 | 0.0162618 | intron-variant | CHD4 | GRCh38.p7 | 12:6595285 | TTAGACTGCAGCAAA[A/G]ATACATTGTCCTACC | 1108 |
| rs115927377 | snp | C/T | 0.000708816 | 0.0188124 | intron-variant | CHD4 | GRCh38.p7 | 12:6570732 | CAGAATTCCAGATGA[C/T]AGGAATCCACCCAAT | 1108 |
| rs115997990 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | CHD4 | GRCh38.p7 | 12:6572856 | TGAGCCACCGCGCCC[A/G]GCCAGGAGTCCATCT | 1108 |
| rs116114545 | snp | A/G | 0.0364509 | 0.129988 | intron-variant | CHD4 | GRCh38.p7 | 12:6585108 | CAACTGAAAGAACCC[A/G]GAGCTGAGTGGTTTA | 1108 |
| rs116233002 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CHD4 | GRCh38.p7 | 12:6587120 | AAGGTTTAATAAAAC[A/T]CATAGGAGAAAATGA | 1108 |
| rs116292242 | snp | A/T | 0.0123036 | 0.0774623 | intron-variant | CHD4 | GRCh38.p7 | 12:6585590 | TCTGGCCCAATTCTA[A/T]TCTTTAAAAAAACAT | 1108 |
| rs116460731 | snp | A/C/G | 0.0180829 | 0.0933524 | intron-variant | CHD4 | GRCh38.p7 | 12:6570710 | TAGAGAAGGAGACCC[A/C/G]AGGAGTCAGAATTCC | 1108 |
| rs116633312 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | CHD4 | GRCh38.p7 | 12:6588225 | ATTCCAGATGGTGGA[A/G]CCCTCATAGAGGCCA | 1108 |
| rs116695160 | snp | A/G | 0.011694 | 0.0755661 | intron-variant | CHD4 | GRCh38.p7 | 12:6593393 | AACTCTTTCTCTAGG[A/G]TGGCTTCCCTCCCCT | 1108 |
| rs116817515 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | CHD4 | GRCh38.p7 | 12:6589805 | CATCATCACCTCTGT[A/G]GCATTCTTGCCCAGA | 1108 |
| rs116849726 | snp | A/G | 0.00126925 | 0.0251598 | synonymous-codon | CHD4 | GRCh38.p7 | 12:6596038 | CTGCTTGAACAGGTC[A/G]TAATCCTGGATCTCC | 1108 |
| rs116999178 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant, upstream-variant-2KB | CHD4, SCARNA11 | GRCh38.p7 | 12:6583551 | TTGAGAGTACACAGC[G/T]CCTCATAATTACATA | 1108 |
| rs117336880 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CHD4 | GRCh38.p7 | 12:6575960 | TACCAAAAAAATCTC[C/T]GTCGCATTCTTCAAA | 1108 |
| rs117440279 | snp | A/G | 0.0154538 | 0.0865337 | upstream-variant-2KB | CHD4 | GRCh38.p7 | 12:6609310 | AGAGAACATATCCCA[A/G]TAAGATTTATCGTGG | 1108 |
| rs117704091 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CHD4 | GRCh38.p7 | 12:6571508 | TGCTTTGCTTTCCAT[C/T]TCAAGAACCTGAATA | 1108 |
| rs117774291 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | CHD4 | GRCh38.p7 | 12:6587261 | TTCAAAGGAAGAGGA[G/T]CAATTCATCAACATA | 1108 |
| rs118040464 | snp | C/T | 0.0376037 | 0.131863 | intron-variant | CHD4 | GRCh38.p7 | 12:6589063 | GACTAAGCTGGCCAA[C/T]GTGGTGAAACCCTGC | 1108 |
| rs137922586 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | CHD4 | GRCh38.p7 | 12:6596963 | GACTCTGTCTCAAAA[A/G]ATATAATAAATAAAT | 1108 |
| rs137971621 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CHD4 | GRCh38.p7 | 12:6605272 | AGCAGAAGGAATGAA[A/G]AAATGACATGTAGAA | 1108 |
| rs138116135 | snp | A/G | 0.000117634 | 0.00766833 | missense | CHD4 | GRCh38.p7 | 12:6602094 | CCTCACTGTCTGAGC[A/G]CAGAGCCACCTCTTC | 1108 |
| rs138250427 | snp | G/T | 0.000296511 | 0.0121724 | synonymous-codon | CHD4 | GRCh38.p7 | 12:6593533 | TACGACATACATGTC[G/T]GGAGCCCACATTTCA | 1108 |
| rs138428898 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | CHD4 | GRCh38.p7 | 12:6584366 | AAATTGTTAGAGGAC[A/G]GGAGAGAAAAGAGAT | 1108 |
| rs138502110 | in-del | -/GC | 0.00438332 | 0.0466095 | upstream-variant-2KB | CHD4 | GRCh38.p7 | 12:6608280 | CCATAATGATCAACA[-/GC]CCTACTGTCGCCCCA | 1108 |
| rs138598843 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CHD4 | GRCh38.p7 | 12:6590847 | AAAACAAAACAGGCT[A/G]GGCGTGGTGGCTCGT | 1108 |
| rs138642107 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6600163 | CCCGAAGAGCTTTAC[C/T]GTCCCACCCTTCTTC | 1108 |
| rs138722881 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CHD4 | GRCh38.p7 | 12:6596699 | CAGCTACTCGGGAAG[A/C]TGAAGCAGGAGAATT | 1108 |
| rs138784875 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | CHD4 | GRCh38.p7 | 12:6605511 | ATAGCGTAACCCCTA[A/G]CACACCTACACAGAC | 1108 |
| rs138856908 | snp | A/G | 0.000494381 | 0.0157145 | synonymous-codon | CHD4 | GRCh38.p7 | 12:6596083 | CCAAGAAGCCTGATC[A/G]TAAGGTAAGTCCCGC | 1108 |
| rs138908518 | snp | A/C/T | 0.00517822 | 0.0506191 | intron-variant | CHD4 | GRCh38.p7 | 12:6590279 | TAACTAAATGGAACA[A/C/T]GGGACCTGGGATTGG | 1108 |
| rs138912992 | snp | C/G/T | 6.82855e-05 | 0.00584284 | missense | CHD4 | GRCh38.p7 | 12:6606282 | ATGTTACCTGGGTGG[C/G/T]GTGGGGGCAGGCTGT | 1108 |
| rs138939193 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon, downstream-variant-500B | CHD4, SCARNA11 | GRCh38.p7 | 12:6581369 | TTTGAGGCTATTTTC[C/T]TCTATTTTTATCCCA | 1108 |
| rs138984606 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CHD4 | GRCh38.p7 | 12:6574495 | TTAATTTATGAAAAG[A/T]TTTTAATTACTTAAA | 1108 |
| rs138993779 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | CHD4 | GRCh38.p7 | 12:6584620 | AACTCCTGGGCTCAA[A/G]CGACCCTCCTGCCTC | 1108 |
| rs139015656 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant | CHD4 | GRCh38.p7 | 12:6584299 | CACATAAAATATTTT[G/T]GGAAAGATATAAAAG | 1108 |
| rs139079695 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | CHD4 | GRCh38.p7 | 12:6571548 | TTAAAAGAGGTGGCC[A/G]GGTGCAGTGGCTCAC | 1108 |
| rs139129663 | snp | C/G | 0.178144 | 0.239451 | intron-variant | CHD4 | GRCh38.p7 | 12:6579680 | CACTTGAACCCAGGA[C/G]GCGGAGGTTGCAGTG | 1108 |
| rs139187379 | snp | A/G | 6.58892e-05 | 0.00573936 | synonymous-codon | CHD4 | GRCh38.p7 | 12:6587761 | AGTGCCAAATTTGAG[A/G]ATATCATCAAGCTCC | 1108 |
| rs139223495 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | CHD4 | GRCh38.p7 | 12:6588221 | CCTAATTCCAGATGG[C/T]GGAGCCCTCATAGAG | 1108 |
| rs139403257 | in-del | -/A/C | | | upstream-variant-2KB | CHD4 | GRCh38.p7 | 12:6607592 | GCCACGCCCCCTTCG[-/A/C]CAGCGGGCGCGCGCG | 1108 |
| rs139506717 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | CHD4 | GRCh38.p7 | 12:6609137 | AGCAAGGCCGAGCTC[C/T]GCACCATGGAGAATC | 1108 |
| rs139536996 | snp | C/T | 6.58946e-05 | 0.0057396 | synonymous-codon | CHD4 | GRCh38.p7 | 12:6599980 | ACCCTCCGAATTGTC[C/T]TCTTTAGCTTCCCAC | 1108 |
| rs139582113 | snp | G/T | 1.64762e-05 | 0.00287016 | intron-variant | CHD4 | GRCh38.p7 | 12:6591651 | CTTAGGTCACTAAGG[G/T]TTGTCTATGACTGTT | 1108 |
| rs139597116 | snp | C/T | 0.00260249 | 0.0359788 | intron-variant | CHD4 | GRCh38.p7 | 12:6597869 | CCCACGGAGACTGCC[C/T]GTCTCCCGTGTGCTC | 1108 |
| rs139646701 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6593810 | GTCCCACCATAACTA[C/T]AAGTCTTACCTCTCC | 1108 |
| rs139702202 | snp | A/G | 0.0398339 | 0.135399 | intron-variant | CHD4 | GRCh38.p7 | 12:6598430 | AGAGCTGGACACTGA[A/G]AGAAAAAGAGACAAC | 1108 |
| rs139854365 | snp | A/G/T | 6.59624e-05 | 0.0057426 | intron-variant, nc-transcript-variant | CHD4, SCARNA11 | GRCh38.p7 | 12:6581517 | CCCTATTCTTAGGAC[A/G/T]GCCCTCCTAAACTGA | 1108 |
| rs139888449 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CHD4 | GRCh38.p7 | 12:6576458 | TAGCTGGAACTACAG[A/G]TGCACGCCACCAGAA | 1108 |
| rs139897273 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CHD4 | GRCh38.p7 | 12:6606218 | TCACCAGAGGAGTCA[C/T]TCGGGAGAGCCCCAG | 1108 |
| rs139947408 | in-del | -/A/C | | | upstream-variant-2KB | CHD4 | GRCh38.p7 | 12:6608051 | GAAACTCACCCCCCC[-/A/C]CCATACTACAACAAC | 1108 |
| rs140244054 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | CHD4 | GRCh38.p7 | 12:6598582 | TTGGGAGGCCGAGGC[A/G]GGCAGATCACGAGGT | 1108 |
| rs140310453 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6588060 | AGGTCCACAGCCTAC[A/T]TTCATAGGAAACTTC | 1108 |
| rs140376282 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6604932 | TTTCTCATGCCCCTC[C/T]CAGAAGGACAGGGTC | 1108 |
| rs140385212 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | CHD4 | GRCh38.p7 | 12:6577294 | GGGTGTGGTGGCAGG[C/T]GCCTGTAATCTCAGC | 1108 |
| rs140410250 | snp | C/T | 1.64732e-05 | 0.0028699 | missense | CHD4 | GRCh38.p7 | 12:6591918 | TGGCACTACATACCA[C/T]TGCAGCCACAGGGAA | 1108 |
| rs140585746 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CHD4 | GRCh38.p7 | 12:6585349 | GAGTGCAGTGGGGCA[A/G]TCTTGGCTCACTGCA | 1108 |
| rs140699855 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CHD4 | GRCh38.p7 | 12:6586769 | GTGGCGCAATCTCAG[C/T]TCATTGCAACCTCCG | 1108 |
| rs140718531 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CHD4 | GRCh38.p7 | 12:6599607 | TTTGAAGTTAGTCCT[A/G]TATTTTCCCAGGACA | 1108 |
| rs140924691 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CHD4 | GRCh38.p7 | 12:6603714 | GAGACAAACATGAAG[A/G]TAATACTAAGAGAAG | 1108 |
| rs141016575 | snp | A/T | 0.0158469 | 0.0875917 | intron-variant | CHD4 | GRCh38.p7 | 12:6586108 | CCGTATCAAAAAAAA[A/T]ATATATAAGGCCAGG | 1108 |
| rs141064180 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | CHD4 | GRCh38.p7 | 12:6606512 | ACTGTCCCCCTCCCC[A/C]ACACCCACCCGCTCT | 1108 |
| rs141170312 | snp | A/G | 0.000153988 | 0.00877328 | missense | CHD4 | GRCh38.p7 | 12:6592697 | AAACACATACTTACT[A/G]GAACCTCTCGGGGGT | 1108 |
| rs141196284 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CHD4 | GRCh38.p7 | 12:6599339 | CTACTCAGCAAGAGG[C/T]TGAGATAGGAGGATC | 1108 |
| rs141301378 | snp | A/G | 0.0029944 | 0.0385776 | synonymous-codon | CHD4 | GRCh38.p7 | 12:6594534 | ATCAGCCAAGATGGT[A/G]TCAGTGCCCTGAGCC | 1108 |
| rs141366600 | snp | C/T | 8.23635e-05 | 0.00641677 | missense | CHD4 | GRCh38.p7 | 12:6601709 | CCTCCTCTGAGAACA[C/T]GTGGTCAATGTCTTC | 1108 |
| rs141382153 | in-del | -/A | | | intron-variant | CHD4 | GRCh38.p7 | 12:6595789 | GCAAGACTTCGTCTC[-/A]AAAAAAAAAAAAAAA | 1108 |
| rs141537775 | in-del | -/G | 3.32718e-05 | 0.00407858 | frameshift-variant | CHD4 | GRCh38.p7 | 12:6600588 | GCGGCTACTACGGCT[-/G]GGTGGAACCATCAGA | 1108 |
| rs141631228 | snp | C/T | 3.51747e-05 | 0.00419358 | missense, upstream-variant-2KB | CHD4, SCARNA11 | GRCh38.p7 | 12:6583027 | AAGCACAGCCCTCAC[C/T]TTCTGAACGTTCATC | 1108 |
| rs141696790 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6587243 | CATGTTATCAGCTTT[C/G]TTTTCAAAGGAAGAG | 1108 |
| rs141735182 | snp | C/G | 0.0418186 | 0.138422 | intron-variant | CHD4 | GRCh38.p7 | 12:6597671 | CTCAGGAGGCTGAGG[C/G]AGGATAATCACTTGA | 1108 |
| rs141751837 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CHD4 | GRCh38.p7 | 12:6595181 | GCTTTCTGATATATA[C/G]AGATGTGGAGAAGTG | 1108 |
| rs141807181 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6591230 | CCTGACCCTTTGCTT[A/G]CCCTCGAGATACAAT | 1108 |
| rs141878949 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHD4 | GRCh38.p7 | 12:6600724 | AAGGGGAAGGACAGA[A/G]TGGCAGAGAGGGGAG | 1108 |
| rs141945658 | snp | A/G | 3.52914e-05 | 0.00420053 | synonymous-codon, upstream-variant-2KB | CHD4, SCARNA11 | GRCh38.p7 | 12:6583094 | ATCGGACTGGTTGTC[A/G]GACTGGTCGTCCTGC | 1108 |
| rs141979439 | snp | A/G | 0.0387552 | 0.1337 | intron-variant | CHD4 | GRCh38.p7 | 12:6580445 | GGCATGGTAGCTCAC[A/G]CCTGTAATCCCAGCA | 1108 |
| rs142136215 | snp | C/T | 0.000399281 | 0.0141238 | missense, downstream-variant-500B | CHD4, SCARNA11 | GRCh38.p7 | 12:6581082 | TCCTCTGTTCTCTCC[C/T]TCACCTCTGCCTTTT | 1108 |
| rs142170234 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | CHD4 | GRCh38.p7 | 12:6579275 | GCCAACATGGTGAAA[C/T]CCTGTCTCTACTAAA | 1108 |
| rs142190841 | in-del | -/CA | 0.00199481 | 0.0315187 | upstream-variant-2KB | CHD4 | GRCh38.p7 | 12:6607976 | TTCAGCCCCATCCCC[-/CA]CAGACATCCCATAAT | 1108 |
| rs142277679 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CHD4 | GRCh38.p7 | 12:6584307 | ATATTTTTGGAAAGA[C/T]ATAAAAGGAACTGAA | 1108 |
| rs142396791 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6573379 | GGTAATAAGAACCTA[A/T]GAAGAACTTCATGGA | 1108 |
| rs142402702 | snp | A/C | 0.0119091 | 0.0762411 | upstream-variant-2KB | CHD4 | GRCh38.p7 | 12:6608205 | TCACATCACCCCCAG[A/C]CTTCCCTCTTCTAGC | 1108 |
| rs142502385 | snp | A/G | 0.000527165 | 0.0162267 | synonymous-codon | CHD4 | GRCh38.p7 | 12:6592736 | TGAGCAGATGAAACA[A/G]CTCTTCCAGATTGTT | 1108 |
| rs142642013 | snp | C/G/T | 6.58897e-05 | 0.00573945 | synonymous-codon, downstream-variant-500B | CHD4, SCARNA11 | GRCh38.p7 | 12:6581111 | TTCCACTTTCTCCTC[C/G/T]CCCTCAGGGGGTTCA | 1108 |
| rs142644691 | snp | A/G | 0.00185122 | 0.0303675 | intron-variant, upstream-variant-2KB | CHD4, SCARNA11 | GRCh38.p7 | 12:6582313 | AGAAAGAGTTAAATA[A/G]GGATCATGCTGACTC | 1108 |
| rs142694233 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CHD4 | GRCh38.p7 | 12:6590878 | GCCTGTAATCCCAGC[A/G]CTTTGGGAGGCCGAG | 1108 |
| rs142800397 | snp | A/G | 0.000148245 | 0.00860815 | synonymous-codon | CHD4 | GRCh38.p7 | 12:6599932 | GTCATCCTCCTCTTC[A/G]AGGTCTCCCCCAACC | 1108 |
| rs142820101 | snp | C/G | 0.000936975 | 0.0216243 | synonymous-codon | CHD4 | GRCh38.p7 | 12:6606287 | ACCTGGGTGGGGTGG[C/G]GGCAGGCTGTTGTTC | 1108 |
| rs142829821 | snp | C/T | 6.71209e-05 | 0.00579275 | synonymous-codon, upstream-variant-2KB | CHD4, SCARNA11 | GRCh38.p7 | 12:6582242 | AGCCCCATCTGCCCC[C/T]GGCTCACATAAATGC | 1108 |
| rs142850933 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CHD4 | GRCh38.p7 | 12:6585878 | CGAGGCAGGCGGATC[A/G]CTTGAGGTCAGGAGT | 1108 |
| rs142859588 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CHD4 | GRCh38.p7 | 12:6588128 | TCATGTTACCCAAAA[C/T]AGGATCACAGCTAAC | 1108 |
| rs142878760 | in-del | -/C | 0.0383715 | 0.133092 | intron-variant | CHD4 | GRCh38.p7 | 12:6590919 | ATGAGGTCAGGAGAT[-/C]CGAGACCATCTTGGC | 1108 |
| rs142952449 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon | CHD4 | GRCh38.p7 | 12:6601049 | CTTCCTCCGAGCATT[A/G]GGACCTAAAATCAGG | 1108 |
| rs143014479 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CHD4 | GRCh38.p7 | 12:6604644 | CAACCCATGGAGGCA[A/G]AGGGGACATCCTTCC | 1108 |
| rs143164031 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | CHD4 | GRCh38.p7 | 12:6577084 | TGGGATTACAGGCGT[C/G]AGCCACCGCACCTGG | 1108 |
| rs143206689 | snp | A/C/G/T | 0.000741027 | 0.0192349 | missense | CHD4 | GRCh38.p7 | 12:6602455 | TTCTTGAGCTTTGGA[A/C/G/T]TCTCTGTTTCTGACA | 1108 |
| rs143259892 | snp | A/T | 0.0123036 | 0.0774623 | intron-variant | CHD4 | GRCh38.p7 | 12:6584288 | TAATTTGTATACACA[A/T]AAAATATTTTTGGAA | 1108 |
| rs143286205 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, downstream-variant-500B | NOP2, CHD4 | GRCh38.p7 | 12:6569993 | GTATCAGGACACCAC[A/G]TAGCCCTTAATTTTC | 1108 |
| rs143362933 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CHD4 | GRCh38.p7 | 12:6587038 | CAGAAAACACAAAGA[G/T]ATAGATTACCTAGGA | 1108 |
| rs143443554 | snp | A/G | 1.64814e-05 | 0.00287061 | missense | CHD4 | GRCh38.p7 | 12:6570891 | GGGGTAGGTTCGGGT[A/G]CCCGGTTTGCCAGGC | 1108 |
| rs143509824 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6599486 | GAAAACATTGTAAGC[C/T]ACCAAGACCCTGAGG | 1108 |
| rs143540075 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6572763 | GACGGGGTTTCACCA[C/T]GTTGGCCAGGCTGGT | 1108 |
| rs143645855 | snp | C/T | 0.00429045 | 0.0461174 | synonymous-codon | CHD4 | GRCh38.p7 | 12:6591919 | GGCACTACATACCAT[C/T]GCAGCCACAGGGAAG | 1108 |
| rs143714564 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6588967 | AAAATGTCAGAATAG[A/G]CCAGGTGCAGTGACT | 1108 |
| rs144001531 | snp | A/G | 3.29473e-05 | 0.00405864 | synonymous-codon | CHD4 | GRCh38.p7 | 12:6587866 | TGCCACCTGCGTGAT[A/G]CGCTCCTCCACTGAC | 1108 |
| rs144061164 | snp | C/T | 0.029116 | 0.117091 | intron-variant | CHD4 | GRCh38.p7 | 12:6571686 | CAAAATTAGCTGGGG[C/T]GCAGTGGCTCATGCC | 1108 |
| rs144069112 | in-del | -/G | 0.000309209 | 0.0124302 | intron-variant | CHD4 | GRCh38.p7 | 12:6594686 | GTCAAGAGCTGGCAA[-/G]GAACTCCCCTCCTCC | 1108 |
| rs144146704 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CHD4 | GRCh38.p7 | 12:6597423 | ATGAGCAGTGATCAC[A/G]ACACTGCACTCAAGC | 1108 |
| rs144201113 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6593827 | AGTCTTACCTCTCCC[A/G]TTAAGTCTTTATATA | 1108 |
| rs144216235 | snp | A/G | 3.30393e-05 | 0.0040643 | synonymous-codon | CHD4 | GRCh38.p7 | 12:6578913 | CTTCTCTACATCAGC[A/G]GCACCTAGGGGAAGA | 1108 |
| rs144286273 | snp | C/T | 1.6473e-05 | 0.00286988 | synonymous-codon | CHD4 | GRCh38.p7 | 12:6601707 | ATCCTCCTCTGAGAA[C/T]ACGTGGTCAATGTCT | 1108 |
| rs144328307 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CHD4 | GRCh38.p7 | 12:6575897 | TAAGCTTTGCTGGCT[C/T]ACATCTTTGCCCAAC | 1108 |
| rs144330964 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHD4 | GRCh38.p7 | 12:6598161 | CCTTCTATCCACAAG[A/G]CTCTTTTGTCACTAT | 1108 |
| rs144404151 | snp | A/G | 1.65932e-05 | 0.00288034 | intron-variant, upstream-variant-2KB | CHD4, SCARNA11 | GRCh38.p7 | 12:6582770 | GAAGAAGAAACCCAG[A/G]TGAGAGGCAGCAGGT | 1108 |
| rs144550882 | snp | A/G | 1.64746e-05 | 0.00287002 | synonymous-codon | CHD4 | GRCh38.p7 | 12:6570917 | CAGGCGGCTGAGAAT[A/G]TTACGCTCTGACATC | 1108 |
| rs144661331 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | CHD4 | GRCh38.p7 | 12:6605812 | GATCAGAAGCTAAAA[A/G]TAATCAGATAGAGTG | 1108 |
| rs144662304 | snp | A/G | 0.00042871 | 0.0146346 | synonymous-codon | CHD4 | GRCh38.p7 | 12:6597986 | AAATTTAGGGTCCTT[A/G]TTCTTTCGCTTTCGG | 1108 |
| rs144833873 | snp | A/T | | | intron-variant | CHD4 | GRCh38.p7 | 12:6603725 | GAAGGTAATACTAAG[A/T]GAAGAACTCGATCAC | 1108 |
| rs144858755 | in-del | -/AT | 0.0142736 | 0.0832652 | intron-variant | CHD4 | GRCh38.p7 | 12:6574322 | CCATGATATGAATAC[-/AT]GTTTCACCTATGCAT | 1108 |
| rs144876223 | snp | C/T | 0.000594128 | 0.0172253 | missense, intron-variant | CHD4 | GRCh38.p7 | 12:6600395 | GTCACCTCCTCCTCG[C/T]CTGGGCAAGGAAGAG | 1108 |
| rs144943071 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | CHD4 | GRCh38.p7 | 12:6604201 | AATCGCTTGAGCCCG[A/G]GAGGCGGAGGTTGCA | 1108 |
| rs144986034 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6578347 | CTGTACCGTGGTTTC[C/T]GACAAGAACCCCAAT | 1108 |
| rs145095645 | snp | A/G | 8.23676e-05 | 0.00641693 | synonymous-codon | CHD4 | GRCh38.p7 | 12:6601749 | GTCTTCCAGGAGCTG[A/G]GCAGATGATTTAGGC | 1108 |
| rs145151103 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CHD4 | GRCh38.p7 | 12:6583657 | TGCTTTCTTCTAACC[C/T]CTTGCACTGATGCAT | 1108 |
| rs145435159 | snp | C/T | 1.73492e-05 | 0.00294522 | missense | CHD4 | GRCh38.p7 | 12:6601047 | GGCTTCCTCCGAGCA[C/T]TGGGACCTAAAATCA | 1108 |
| rs145463385 | in-del | -/AACAACAAC | | | intron-variant | CHD4 | GRCh38.p7 | 12:6580230 | AGACTCCATCTCGAA[-/AACAACAAC]AACAACAACAACAAC | 1108 |
| rs145532596 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | CHD4 | GRCh38.p7 | 12:6598855 | AAATCTAATCCCAGG[A/T]CTCCTCCAGGGAGAA | 1108 |
| rs145681539 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CHD4 | GRCh38.p7 | 12:6602300 | AGAAAGAAACAAATG[C/T]CCTCAGCCCTTCAAC | 1108 |
| rs145780917 | snp | C/G | 0.0154538 | 0.0865337 | | | GRCh38.p7 | 12:6584360 | GGAACTAAATTGTTA[C/G]AGGACAGGAGAGAAA | 1108 |
| rs145869742 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | CHD4 | GRCh38.p7 | 12:6598576 | AGCACCTTGGGAGGC[C/T]GAGGCGGGCAGATCA | 1108 |
| rs145892046 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6590815 | GGCAACAGAGTGAGA[A/C]CCTATCTCGAATAAA | 1108 |
| rs146063884 | snp | C/T | 1.66051e-05 | 0.00288137 | synonymous-codon, upstream-variant-2KB | CHD4, SCARNA11 | GRCh38.p7 | 12:6582908 | ATCTTTATCATTCCG[C/T]AGGCCCTTACGACTG | 1108 |
| rs146256690 | snp | C/T | 0.0383715 | 0.133092 | intron-variant | CHD4 | GRCh38.p7 | 12:6597722 | AGTGAGCCGAGATCA[C/T]GCCACTGCACTCCAG | 1108 |
| rs146335849 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | CHD4 | GRCh38.p7 | 12:6592915 | CCCAATAGTTAAGCA[A/T]CCCACTCCTCACATT | 1108 |
| rs146415271 | snp | A/C | 0.0349115 | 0.127424 | intron-variant | CHD4 | GRCh38.p7 | 12:6571964 | AAAACTCCATCTCAA[A/C]AAACAAACAAAAAAA | 1108 |
| rs146656617 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB | CHD4 | GRCh38.p7 | 12:6609322 | CCAATAAGATTTATC[A/G]TGGTCCTTCTAGAGG | 1108 |
| rs146797810 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CHD4 | GRCh38.p7 | 12:6586277 | TGGAGGCAGGCACCT[A/G]TAGTCCCCAGCTACT | 1108 |
| rs147099416 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | CHD4 | GRCh38.p7 | 12:6596441 | GATCGCTTGAGGCCA[A/G]GAGCTCAAGACCAGC | 1108 |
| rs147135592 | snp | A/G | 0.00258612 | 0.035866 | intron-variant | CHD4 | GRCh38.p7 | 12:6587955 | TGCTAAAGGCCTGGA[A/G]TTGAACAGGAAATAA | 1108 |
| rs147152222 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6584923 | TCTGATTGAACACTA[C/T]GGTACACAGACCTAT | 1108 |
| rs147241331 | snp | C/G | 0.0126979 | 0.078662 | upstream-variant-2KB, downstream-variant-500B | NOP2, CHD4 | GRCh38.p7 | 12:6569627 | TTCAAGGTTGGAGGA[C/G]GTTAGGTCGGGCCTC | 1108 |
| rs147387698 | snp | A/C/G | 6.58917e-05 | 0.00573952 | missense | CHD4 | GRCh38.p7 | 12:6599972 | ATCTCCTCACCCTCC[A/C/G]AATTGTCCTCTTTAG | 1108 |
| rs147397787 | snp | A/G | 6.81211e-05 | 0.00583574 | missense | CHD4 | GRCh38.p7 | 12:6606336 | TCCTCCTCACTGCCC[A/G]CCGAGCAGGGGGACG | 1108 |
| rs147434366 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CHD4 | GRCh38.p7 | 12:6588143 | TAGGATCACAGCTAA[C/G]CAAACTCTGGCTTAC | 1108 |
| rs147536921 | snp | A/C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, downstream-variant-500B | NOP2, CHD4 | GRCh38.p7 | 12:6570043 | TCCTGCCGCACACAC[A/C/T]CATCCACCTGCACCT | 1108 |
| rs147588825 | in-del | -/TTAAT | 0.0166325 | 0.0896639 | intron-variant | CHD4 | GRCh38.p7 | 12:6574480 | GCAGAATGTTGGTTC[-/TTAAT]TTATGAAAAGATTTT | 1108 |
| rs147712453 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6603052 | GTGCCAGCTCAATCT[C/G]ATGCCCACTTCTAAA | 1108 |
| rs147729068 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHD4 | GRCh38.p7 | 12:6599094 | CAGACTTAGAGCACA[A/G]AATTCCTCCCTTAAG | 1108 |
| rs147764696 | in-del | -/C | 0.448452 | 0.152042 | intron-variant | CHD4 | GRCh38.p7 | 12:6572655 | TCCGCCTCCCGGGTT[-/C]CAAGCGATTCTCCTG | 1108 |
| rs147796962 | snp | C/T | 6.59696e-05 | 0.00574286 | synonymous-codon | CHD4 | GRCh38.p7 | 12:6592485 | CCGCCGCAACATGTG[C/T]GGCCCCAGCATGTCA | 1108 |
| rs147831032 | snp | C/G/T | 0.00343288 | 0.041288 | intron-variant, upstream-variant-2KB | CHD4, SCARNA11 | GRCh38.p7 | 12:6582802 | GCATTCCACCAAAGA[C/G/T]GCAATATCTGACACT | 1108 |
| rs148055188 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6591217 | AGCTTGAACAAGTCC[G/T]GACCCTTTGCTTGCC | 1108 |
| rs148063992 | snp | C/T | 4.95201e-05 | 0.0049757 | synonymous-codon | CHD4 | GRCh38.p7 | 12:6598270 | AGACATGCCTTGCCA[C/T]TTCACAAAGAACTGC | 1108 |
| rs148095286 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6580337 | ATTCTTCAGTGTGTC[A/G]CTTCCTCCTGATATC | 1108 |
| rs148235976 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6597481 | AAAATAAATATATAA[A/G]GCTGAGCGTGGTGGC | 1108 |
| rs148372288 | in-del | -/A | | | intron-variant, downstream-variant-500B | CHD4, SCARNA11 | GRCh38.p7 | 12:6581017 | TCAAAACAAACAAAC[-/A]AAACAAAAAAAATGT | 1108 |
| rs148408747 | snp | A/G | 0.000155522 | 0.00881686 | intron-variant, upstream-variant-2KB | CHD4, SCARNA11 | GRCh38.p7 | 12:6582284 | AGAGACATATGCCCT[A/G]TGTAAAGAAGTAGAG | 1108 |
| rs148460516 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | CHD4 | GRCh38.p7 | 12:6585824 | ACAAAGAGGCCAGGC[A/G]TAATGGCTCATGCCT | 1108 |
| rs148549138 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, downstream-variant-500B | NOP2, CHD4 | GRCh38.p7 | 12:6570066 | CTGCACCTACACCCA[A/C]ACTGAACCAGAGCAC | 1108 |
| rs148588653 | snp | A/C | 0.000171101 | 0.00924777 | missense | CHD4 | GRCh38.p7 | 12:6601027 | GTACACGAGGGCTGC[A/C]CTTGGGCTTCCTCCG | 1108 |
| rs148670709 | in-del | -/G | | | intron-variant | CHD4 | GRCh38.p7 | 12:6603567 | GAGAGGTGGGGTGGC[-/G]GGGGGGGGAGACTGC | 1108 |
| rs148705976 | snp | A/C/G | 0.000181293 | 0.00951936 | intron-variant | CHD4 | GRCh38.p7 | 12:6601772 | ATTTAGGCTCCTGCA[A/C/G]AAAGAGCAAAGTCAA | 1108 |
| rs148739914 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6588952 | CCTAACTCTTATAGA[A/C]AAATGTCAGAATAGG | 1108 |
| rs148990354 | snp | A/G | 0.000457662 | 0.0151202 | synonymous-codon, upstream-variant-2KB | CHD4, SCARNA11 | GRCh38.p7 | 12:6581695 | CTGCGTGTCCCCTGG[A/G]GTGGAGGGTGTAGGA | 1108 |
| rs149049733 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6590668 | TACAAAAAAATTTTT[G/T]TAGTTAGCTAGGTAC | 1108 |
| rs149071560 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6604298 | AAAGAAAATAATATC[C/T]CTCCTTCAATCCCTG | 1108 |
| rs149141715 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6583857 | AACGAAAAGAATTCT[A/G]TATAGCCTCTTATGT | 1108 |
| rs149214000 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | CHD4 | GRCh38.p7 | 12:6594132 | GAGCCACTGCGTCCA[A/G]CCAAGCCTTTCCATA | 1108 |
| rs149386734 | snp | A/T | 0.0103295 | 0.0711199 | intron-variant | CHD4 | GRCh38.p7 | 12:6605775 | CTTCACACAGTTCAG[A/T]CAGCACAGAAAACCG | 1108 |
| rs149454833 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6584673 | CTAGGCATGAGCCAC[C/T]GTGTCTGGCCCTTTT | 1108 |
| rs149561722 | snp | A/C | 1.66112e-05 | 0.00288189 | missense, intron-variant | CHD4 | GRCh38.p7 | 12:6602163 | CCCCCAGCTGCCGGC[A/C]TAAGAGCATACGCTG | 1108 |
| rs149616957 | snp | A/G | | | intron-variant | CHD4 | GRCh38.p7 | 12:6586853 | CAGGTGTGCTTCATC[A/G]TGCCTGGCTAATTTT | 1108 |
| rs149647102 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHD4 | GRCh38.p7 | 12:6575632 | TTAACACCTCATGAT[C/T]ATATGACAGTTTTAT | 1108 |
| rs149696821 | snp | A/G | | | upstream-variant-2KB | CHD4 | GRCh38.p7 | 12:6609296 | CCACTGGTTCCAAGA[A/G]AGAACATATCCCAAT | 1108 |
| rs149702292 | snp | A/C | 8.25171e-05 | 0.00642275 | intron-variant, upstream-variant-2KB | CHD4, SCARNA11 | GRCh38.p7 | 12:6581622 | CAAAAAGAGAGGGAC[A/C]GAAAATGATAGGACA | 1108 |
| rs149838772 | snp | C/G | 0.0460142 | 0.144533 | intron-variant | CHD4 | GRCh38.p7 | 12:6598558 | GCTCATGCCTGAAAT[C/G]CCAGCACCTTGGGAG | 1108 |
| rs149884399 | snp | C/T | 0.000428534 | 0.0146316 | synonymous-codon | CHD4 | GRCh38.p7 | 12:6600250 | CTTGCCCTCGGGAGC[C/T]TTCTCCATGTCGGGA | 1108 |
| rs149894463 | snp | A/C | 0.0123036 | 0.0774623 | intron-variant | CHD4 | GRCh38.p7 | 12:6604032 | CCTGTAATCGCAGCA[A/C]TCTGGGAGGCTGAGG | 1108 |
| rs149936307 | snp | C/G/T | 6.58907e-05 | 0.00573948 | synonymous-codon | CHD4 | GRCh38.p7 | 12:6587830 | CCGCACCACTAGATG[C/G/T]GTCAGCATCATTTTC | 1108 |
| rs149961532 | snp | A/G | 0.000630036 | 0.0177376 | synonymous-codon | CHD4 | GRCh38.p7 | 12:6578079 | TCGATGCCAGATCTC[A/G]TAAGTCTTCTTGGTA | 1108 |
| rs150098926 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6600147 | CCATTTCCATCCAGG[C/T]CCCGAAGAGCTTTAC | 1108 |
| rs150135724 | in-del | -/AAAC | 0.000401912 | 0.0141702 | intron-variant, downstream-variant-500B | CHD4, SCARNA11 | GRCh38.p7 | 12:6581004 | CACTACACTGTCTCA[-/AAAC]AAACAAACAAACAAA | 1108 |
| rs150187989 | snp | A/G | 0.0562307 | 0.157967 | intron-variant | CHD4 | GRCh38.p7 | 12:6586137 | GGGGCAGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 1108 |
| rs150239341 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant | CHD4 | GRCh38.p7 | 12:6590190 | GCAACAGAGTGAGAC[G/T]CCATCCCGAAGAAGA | 1108 |
| rs150271314 | in-del | -/A | | | intron-variant | CHD4 | GRCh38.p7 | 12:6597120 | AAAAATACAAAAAAA[-/A]AAAAAATTAGCCAGG | 1108 |
| rs150404906 | snp | C/T | 0.000201925 | 0.010046 | missense | CHD4 | GRCh38.p7 | 12:6602093 | CCCTCACTGTCTGAG[C/T]GCAGAGCCACCTCTT | 1108 |
| rs150432752 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CHD4, SCARNA11 | GRCh38.p7 | 12:6583527 | CCTAAGAACTTAGAA[G/T]AAATTTGATTGAGAG | 1108 |
| rs150460854 | snp | A/C | 0.000153988 | 0.00877328 | missense | CHD4 | GRCh38.p7 | 12:6593138 | CATCCACGATGAGGC[A/C]GGCCCAATCAATAGA | 1108 |
| rs150553552 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | CHD4 | GRCh38.p7 | 12:6591247 | CCTCGAGATACAATG[C/G]TTTCTTCTTTCTAGC | 1108 |
| rs150605497 | snp | A/G | 0.000661989 | 0.0181812 | intron-variant | CHD4 | GRCh38.p7 | 12:6598187 | ACTATCCTCTTCATC[A/G]TAGCCCCTACATCTC | 1108 |
| rs150745878 | snp | A/G | | | intron-variant | CHD4 | GRCh38.p7 | 12:6584521 | CTCCCACGCAGCTGG[A/G]ACCACAAGCGTGAGC | 1108 |
| rs150806437 | snp | A/G | 0.000131778 | 0.00811614 | synonymous-codon | CHD4 | GRCh38.p7 | 12:6587516 | AATGGCCTTATCATC[A/G]TAGTGGATAACACTG | 1108 |
| rs150832622 | snp | A/C | 0.000426288 | 0.0145932 | missense | CHD4 | GRCh38.p7 | 12:6601984 | ATCATCATCATCCTC[A/C]TCCTCCTCCTCCTCC | 1108 |
| rs150834899 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | CHD4 | GRCh38.p7 | 12:6575314 | TTAGTCAGGCATGGT[A/G]GTACATGCCTGTAAT | 1108 |
| rs150885232 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | CHD4 | GRCh38.p7 | 12:6608455 | CCAGTGTCACATCCC[A/G]TAATGCTTCATCTCC | 1108 |
| rs150919087 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6599569 | CTCCTCTTAAGAGAG[A/C]TGGCAAAACATCAAC | 1108 |
| rs151101744 | snp | A/G | 1.65154e-05 | 0.00287358 | intron-variant | CHD4 | GRCh38.p7 | 12:6570841 | GGTTCTGCAGGAAGA[A/G]GTGGTGTCAAGAAGA | 1108 |
| rs151150853 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6577144 | AAGAACCAGGCCAGG[A/C]ATGGTGGCTCATGCC | 1108 |
| rs151292235 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CHD4 | GRCh38.p7 | 12:6594886 | ACTGAGGAAAAGCAC[A/G]TCACAGACTCCCTAC | 1108 |
| rs151333693 | snp | A/G | 1.65018e-05 | 0.00287239 | synonymous-codon | CHD4 | GRCh38.p7 | 12:6593130 | ATGGGCTTCATCCAC[A/G]ATGAGGCAGGCCCAA | 1108 |
| rs180954439 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | CHD4 | GRCh38.p7 | 12:6597734 | TCACGCCACTGCACT[A/C]CAGCCTGGGCACAGA | 1108 |
| rs181144039 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | CHD4 | GRCh38.p7 | 12:6578350 | TACCGTGGTTTCTGA[A/C]AAGAACCCCAATTTC | 1108 |
| rs181159969 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | CHD4 | GRCh38.p7 | 12:6598843 | TCATTTCAAATAAAA[A/T]CTAATCCCAGGACTC | 1108 |
| rs181169168 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHD4 | GRCh38.p7 | 12:6587177 | GTTGTGAGCATGATA[C/T]TTGGTTGTAAGTTTT | 1108 |
| rs181367339 | snp | A/G | 0.000481148 | 0.015503 | intron-variant, upstream-variant-2KB | CHD4, SCARNA11 | GRCh38.p7 | 12:6582774 | AAGAAACCCAGGTGA[A/G]AGGCAGCAGGTCGCA | 1108 |
| rs181456215 | snp | C/T | | | intron-variant | CHD4 | GRCh38.p7 | 12:6594965 | TGTCCCTCTTAGATT[C/T]ATCTTTTTAACTTTA | 1108 |
| rs181587159 | snp | C/G | | | intron-variant | CHD4 | GRCh38.p7 | 12:6603569 | GAGGTGGGGTGGCGG[C/G]GGGGGAGACTGCCCT | 1108 |
| rs181591590 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CHD4 | GRCh38.p7 | 12:6574028 | ACTGTCTCAAAAAAA[A/T]AGGGGTTATTTTGCT | 1108 |
| rs181601826 | snp | A/T | | | intron-variant | CHD4 | GRCh38.p7 | 12:6603935 | ATTCCTATCCAACAT[A/T]TGGGAATGTCTGCAC | 1108 |
| rs181634517 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CHD4 | GRCh38.p7 | 12:6584230 | AAAAAAAGTCTTTGG[G/T]TACATATATGTGAGT | 1108 |
| rs181700752 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHD4 | GRCh38.p7 | 12:6572548 | CCCACCTGGGCAAAA[C/T]GGTGAGAGCCCATCT | 1108 |
| rs181766401 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHD4 | GRCh38.p7 | 12:6573396 | AAGAACTTCATGGAC[A/G]GCTCATTCCCACACC | 1108 |
| rs181769374 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | CHD4 | GRCh38.p7 | 12:6594084 | AGGTGATCCACCAAC[C/G]TCGGGCTTCCAAAGT | 1108 |
| rs181959973 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | CHD4 | GRCh38.p7 | 12:6577203 | GCAGGTGGATCACTT[C/T]GAGGTCAGGAGTTTG | 1108 |
| rs181976036 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6597327 | CATGAAGTGTCAGGC[A/G]CAGTAGCTCACGCCT | 1108 |
| rs182008136 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6593857 | ACTTTTTTTCTGAGA[C/T]GGAGTTTCACTCTTG | 1108 |
| rs182212911 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6589310 | AAACAGGACACTGAC[A/G]TAGTCTCAAATATCT | 1108 |
| rs182313873 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6588941 | CAGAGCAAGACCCTA[A/C]CTCTTATAGAAAAAT | 1108 |
| rs182457626 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CHD4 | GRCh38.p7 | 12:6600730 | AAGGACAGAGTGGCA[A/G]AGAGGGGAGTACTCT | 1108 |
| rs182592969 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CHD4 | GRCh38.p7 | 12:6609108 | TTCATTCAACCTGTG[C/T]TGACAGAGTACCTAG | 1108 |
| rs182594662 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6580139 | GGCTGAGGCAGGAGA[A/G]TCGCTTGAACCCAGG | 1108 |
| rs182675615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6584794 | AAGAACAATTTGTAT[A/G]CTTATGTAGTCACCA | 1108 |
| rs182677214 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6604727 | AACCGCAAACTTACT[A/G]AGATATAGAGAAGAT | 1108 |
| rs182911355 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB, downstream-variant-500B | NOP2, CHD4 | GRCh38.p7 | 12:6569913 | CCTCTCATTTTCCAC[A/C]GGTGGAAGTCAACGT | 1108 |
| rs182935912 | snp | A/G | 0.000385192 | 0.0138725 | intron-variant | CHD4 | GRCh38.p7 | 12:6600192 | TCTCATGGGTTCCAA[A/G]GGGCCACAATGGCCA | 1108 |
| rs182970303 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6605247 | GCTCCAGAATGAGAA[A/G]AAAACTAGAAGCAGA | 1108 |
| rs183218996 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | CHD4 | GRCh38.p7 | 12:6590154 | AATGAGTCAAGATCG[C/T]GCCACTGCACTCCAA | 1108 |
| rs183294441 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6595271 | TAAGAGTACCATCAT[C/T]AGACTGCAGCAAAGA | 1108 |
| rs183318102 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | CHD4 | GRCh38.p7 | 12:6575413 | GGAAATGTCGCCACT[A/G]CACTCCAGCCTGGGC | 1108 |
| rs183446903 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6574678 | ATGGGGGTCGGTAGT[A/G]GGAGGGGTGCTGATT | 1108 |
| rs183530894 | snp | A/G | 0.000494894 | 0.0157227 | intron-variant | CHD4 | GRCh38.p7 | 12:6599753 | CCCATTTTTTGCCCC[A/G]GCTGAGATCAGTCAC | 1108 |
| rs183595113 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | CHD4 | GRCh38.p7 | 12:6579180 | ATTAGCTGGGTGCGG[A/T]GGCTCATGCCTGTAA | 1108 |
| rs183651332 | snp | C/T | | | intron-variant | CHD4 | GRCh38.p7 | 12:6586788 | TTGCAACCTCCGCCT[C/T]CTGGGTTCAAGCAAT | 1108 |
| rs183701830 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6595087 | ATGTGGCCCCTCCCC[C/G]CAGACAACACTTCTT | 1108 |
| rs183803644 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | CHD4 | GRCh38.p7 | 12:6604049 | CTGGGAGGCTGAGGC[A/G]GGCAGATCATTTGAG | 1108 |
| rs183877632 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6571834 | GGCATGGTGGCAGGC[A/G]CCTGTAATCCCAGCA | 1108 |
| rs183881071 | snp | C/G | 0.000131807 | 0.00811701 | intron-variant | CHD4 | GRCh38.p7 | 12:6591649 | TCCTTAGGTCACTAA[C/G]GGTTGTCTATGACTG | 1108 |
| rs183893686 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CHD4 | GRCh38.p7 | 12:6580398 | CCATGGTTCACACAG[A/G]GATCTGTAGTGCTTA | 1108 |
| rs183987024 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CHD4 | GRCh38.p7 | 12:6584469 | GAGTGGCGTCATTAC[A/G]GCTCACTGCAGCCTC | 1108 |
| rs184073969 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CHD4 | GRCh38.p7 | 12:6590851 | CAAAACAGGCTGGGC[A/G]TGGTGGCTCGTGCCT | 1108 |
| rs184133418 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHD4 | GRCh38.p7 | 12:6595865 | CAGGAGGCTAAGGCA[A/G]GAGAATCGTTTGAAC | 1108 |
| rs184196040 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6580521 | AGACTGGCCTGACCA[A/T]TATGGAGAAACCCCC | 1108 |
| rs184201825 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CHD4 | GRCh38.p7 | 12:6601860 | GAGTAACAGAGTTAA[A/G]AGGAAAAGAAGAGAA | 1108 |
| rs184205109 | snp | C/G | | | intron-variant | CHD4 | GRCh38.p7 | 12:6571333 | GAATCTGTCTCCCCA[C/G]CTCCATTATAACAGC | 1108 |
| rs184205402 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6572631 | GCACAATCTTGGCTC[A/C]CTGCAAACTCCGCCT | 1108 |
| rs184383245 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CHD4 | GRCh38.p7 | 12:6576674 | GCAGTGGTGCGATCT[C/T]GGCTCACTGCAACCT | 1108 |
| rs184412521 | snp | A/C/G | 1.64811e-05 | 0.00287059 | intron-variant, downstream-variant-500B | CHD4, SCARNA11 | GRCh38.p7 | 12:6581418 | AAGACAATCAATTAG[A/C/G]AAGAAGGTACTAGAT | 1108 |
| rs184544145 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6602635 | GCTATACTCTGTACA[A/G]GAGGAAGCTGATACC | 1108 |
| rs184673335 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6572256 | CATGGTGAAACTCCA[C/T]CTCTACTAAAAATAC | 1108 |
| rs184695240 | snp | A/G | | | intron-variant | CHD4 | GRCh38.p7 | 12:6577241 | CCTAGCCAACATGGT[A/G]AAACCCCATCTCTAC | 1108 |
| rs184695730 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6597456 | GGGCAACACAGCTAA[A/G]ATTTGTCTCAAAATA | 1108 |
| rs184861104 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CHD4 | GRCh38.p7 | 12:6592613 | AGAAGGAGAAAGGAA[G/T]AAAGAAAAGTGATAC | 1108 |
| rs184964881 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6589360 | TCACAATGGGAACAA[C/T]AGAAACTTTACACTG | 1108 |
| rs184986064 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6593980 | AGCTGGGATTACAGG[C/T]GTGCACCACCACATC | 1108 |
| rs185054639 | snp | A/C/G | 0.00557734 | 0.0525397 | intron-variant | CHD4 | GRCh38.p7 | 12:6575726 | TGGCTGCCCATTAAC[A/C/G]ATAGCGTAAAGTCCA | 1108 |
| rs185197241 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6573417 | TTCCCACACCCAAGT[A/C]GTTTAACTTTGCCTT | 1108 |
| rs185210242 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6594202 | CATTCCCCTAGAACT[A/G]ATACTCTATGGATCC | 1108 |
| rs185341437 | snp | C/G | | | intron-variant | CHD4 | GRCh38.p7 | 12:6597227 | CTTGCAGTGAGCCAA[C/G]ATCACGCCACTGCAC | 1108 |
| rs185534357 | snp | C/T | 0.000712405 | 0.0188599 | intron-variant | CHD4 | GRCh38.p7 | 12:6606238 | GAGAGCCCCAGATGT[C/T]TCCTTCCCGCCATGG | 1108 |
| rs185599179 | snp | A/G | 0 | 0 | intron-variant | CHD4 | GRCh38.p7 | 12:6586290 | CTGTAGTCCCCAGCT[A/G]CTCGGGAGGCTGAGG | 1108 |
| rs185662065 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CHD4 | GRCh38.p7 | 12:6603823 | GTCAGCGCATACAAC[C/T]TTCTCCCCAAATTTC | 1108 |
| rs185779196 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CHD4 | GRCh38.p7 | 12:6597756 | GGGCACAGAGTGAGA[C/T]TCTGTCTCAAAAACA | 1108 |
| rs185982137 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6603997 | GAAGAGAATATCCCA[A/G]TCGGGTGCAATGGCT | 1108 |
| rs186056054 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CHD4 | GRCh38.p7 | 12:6584621 | ACTCCTGGGCTCAAA[C/T]GACCCTCCTGCCTCA | 1108 |
| rs186193144 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6599415 | ACTGCACTCTAGCCC[A/G]GATGACAGAATGAGA | 1108 |
| rs186193953 | snp | A/T | | | intron-variant | CHD4 | GRCh38.p7 | 12:6604604 | ATCTCACCACCCCCA[A/T]AAAAGCTGGAAGTGG | 1108 |
| rs186227440 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | CHD4 | GRCh38.p7 | 12:6608564 | CAGTCTATTCTAACA[C/G]CCAGAGCAGGGAGGG | 1108 |
| rs186231319 | snp | C/T | | | missense | CHD4 | GRCh38.p7 | 12:6578855 | ACCCACCTTTGTCTT[C/T]TACCACAATAGGGGT | 1108 |
| rs186313735 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | CHD4 | GRCh38.p7 | 12:6574208 | AGAATGATGTTTTCT[G/T]TATCTATAAAATGCT | 1108 |
| rs186495430 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CHD4 | GRCh38.p7 | 12:6595022 | CAAAACCCAGAGGAA[A/C]TGAGCCTGAATTAAG | 1108 |
| rs186725776 | snp | C/T | 4.99023e-05 | 0.00499486 | intron-variant | CHD4 | GRCh38.p7 | 12:6592063 | GTAGTATTTCCTACA[C/T]GGGCAAGGTAGAAAG | 1108 |
| rs186786277 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CHD4 | GRCh38.p7 | 12:6584320 | GATATAAAAGGAACT[G/T]AAAACATTAGTTGTC | 1108 |
| rs186906512 | snp | A/G | 3.31796e-05 | 0.00407292 | intron-variant | CHD4 | GRCh38.p7 | 12:6588253 | CCACTATGCCTTTCT[A/G]GCATAACATGTTACT | 1108 |
| rs186912301 | snp | G/T | | | intron-variant | CHD4 | GRCh38.p7 | 12:6575489 | TTATTAACCGTTTTT[G/T]GTTTGGGGGGAGAAA | 1108 |
| rs186965658 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6595563 | GAGGCTGAGACGGGC[A/G]GATCACCTGAGGTCA | 1108 |
| rs187045674 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6584855 | CCATCAATCACTTCT[A/G]TTACATTCACTGCCA | 1108 |
| rs187047281 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6604973 | CACCACAACTCCGCC[C/G]TCACCTTGGGCAAGG | 1108 |
| rs187153578 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CHD4 | GRCh38.p7 | 12:6609321 | CCCAATAAGATTTAT[C/T]GTGGTCCTTCTAGAG | 1108 |
| rs187338768 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CHD4 | GRCh38.p7 | 12:6589046 | TGTGGTCAGGAGTTC[A/G]AGACTAAGCTGGCCA | 1108 |
| rs187423799 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | CHD4 | GRCh38.p7 | 12:6575245 | CTGAGGTCCAGAATT[A/T]GAGACCAGCCTGGCC | 1108 |
| rs187427086 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CHD4 | GRCh38.p7 | 12:6595105 | GACAACACTTCTTCA[A/G]TCATTCAAAATATAC | 1108 |
| rs187481499 | snp | A/G | 8.23689e-05 | 0.00641698 | synonymous-codon | CHD4 | GRCh38.p7 | 12:6600322 | CAGGATGATCTCACC[A/G]CCTTGCTGGCACACC | 1108 |
| rs187533752 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6600734 | ACAGAGTGGCAGAGA[A/G]GGGAGTACTCTCTCA | 1108 |
| rs187868678 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CHD4 | GRCh38.p7 | 12:6579568 | CACATCAGCCTGGGC[A/G]ACGGAGCAAGACTCC | 1108 |
| rs187920601 | snp | A/G | 1.64727e-05 | 0.00286986 | missense | CHD4 | GRCh38.p7 | 12:6599835 | GGGGATTCAGGCAGT[A/G]GATGTGGTAGGAAGA | 1108 |
| rs187925835 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHD4 | GRCh38.p7 | 12:6571471 | TTACCTCTAAAGTAT[C/T]GCAAATGACACTGTA | 1108 |
| rs187941508 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHD4 | GRCh38.p7 | 12:6590884 | AATCCCAGCACTTTG[A/G]GAGGCCGAGGTGGGC | 1108 |
| rs188025493 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CHD4 | GRCh38.p7 | 12:6576410 | TAGGCTGGAGTGCAA[C/T]GGCACAATCTAGGCT | 1108 |
| rs188153604 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHD4 | GRCh38.p7 | 12:6571937 | TTGCTCTCCAGCCTG[A/G]GCAACAAGAGCAAAA | 1108 |
| rs188244546 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHD4 | GRCh38.p7 | 12:6605881 | ACAGGATCCTACTAG[C/T]ACAGATGCCCGGCTG | 1108 |
| rs188274374 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6596467 | CCAGCCAGGCCAACA[C/T]GGCGAAACCCGTCTC | 1108 |
| rs188316356 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6597591 | CAGCAGAATGAAAAC[C/T]CTGTCTCTACTAAAA | 1108 |
| rs188489801 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | CHD4 | GRCh38.p7 | 12:6590313 | CTGAAACAGAAAACA[C/G]ACATCAAGAAAAATT | 1108 |
| rs188506936 | snp | C/T | | | intron-variant | CHD4 | GRCh38.p7 | 12:6603899 | TCTCTGAAGCTCAGC[C/T]TCCTCACCACTCCCA | 1108 |
| rs188528105 | snp | C/G | 0.0209421 | 0.100162 | intron-variant | CHD4 | GRCh38.p7 | 12:6585977 | TGGTGGTGCATACCT[C/G]TAATCTCAGCTACTT | 1108 |
| rs188695301 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6587072 | TCTGCCTTTTCTCTA[A/G]AGAGATGAGGTAGCA | 1108 |
| rs188759864 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | CHD4 | GRCh38.p7 | 12:6608295 | GCCCTACTGTCGCCC[C/G]ACAGATGGACATCTA | 1108 |
| rs188771006 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, downstream-variant-500B | NOP2, CHD4 | GRCh38.p7 | 12:6569915 | TCTCATTTTCCACAG[A/G]TGGAAGTCAACGTTG | 1108 |
| rs188867968 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6576708 | CCTCCCGGGTTCAAG[C/T]GATTCTGGAGAACTT | 1108 |
| rs189119184 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6602886 | TAAACCAGGGAATGA[A/G]AATGAAAGATCCTAC | 1108 |
| rs189241423 | snp | A/G | | | intron-variant | CHD4 | GRCh38.p7 | 12:6583740 | AATGGAGAAACTTCT[A/G]AAGTACTGTAAAAGA | 1108 |
| rs189362651 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CHD4 | GRCh38.p7 | 12:6586415 | CAAAATAAATAAATA[A/C]ATACATACATACATA | 1108 |
| rs189395650 | snp | C/T | | | intron-variant, upstream-variant-2KB | CHD4, SCARNA11 | GRCh38.p7 | 12:6582049 | CTCAAGTGATCCACC[C/T]GCCTCAGCCTCCCAA | 1108 |
| rs189403286 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6572792 | GTCTCGAACTCCTGA[C/G]CTCGTGATCCACCTG | 1108 |
| rs189405378 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CHD4 | GRCh38.p7 | 12:6593997 | TGCACCACCACATCC[A/G]GCTAATTTTGTATTT | 1108 |
| rs189606214 | snp | C/T | 0.00133254 | 0.0257778 | utr-variant-5-prime | CHD4 | GRCh38.p7 | 12:6606398 | CTCCCGGCCAGGGAA[C/T]TGGCCCAGCTGCTCC | 1108 |
| rs189617762 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CHD4 | GRCh38.p7 | 12:6577373 | GTTGTAGTGAGCAGA[A/G]GCTGCATCACTGCAT | 1108 |
| rs189633857 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CHD4 | GRCh38.p7 | 12:6594216 | TGATACTCTATGGAT[C/T]CACTGCTAATCCTAC | 1108 |
| rs189692193 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6584774 | GCAGCTATAGTCACT[A/C]ATCAAAGAACAATTT | 1108 |
| rs189899548 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB | CHD4 | GRCh38.p7 | 12:6608779 | AAATCTAGGTATTTT[A/C]CAGATGCTTACCTCC | 1108 |
| rs190139770 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6593254 | AGGCAACTTGGTCAC[C/T]ACTAGTCAGTTCCTC | 1108 |
| rs190147663 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHD4 | GRCh38.p7 | 12:6588515 | GGGGGCAGTGGCTCA[C/T]GCCTGTAATCTCAGC | 1108 |
| rs190156923 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, downstream-variant-500B | NOP2, CHD4 | GRCh38.p7 | 12:6569874 | TCACAGAGCCATTAA[C/G]CGGCGGTGCCCGCAG | 1108 |
| rs190169533 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CHD4 | GRCh38.p7 | 12:6590075 | TGGTGGCACACACCC[A/G]TAATCTCAGCTACTC | 1108 |
| rs190390944 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | CHD4, SCARNA11 | GRCh38.p7 | 12:6580985 | GCACTCCAGCCTGGC[A/G]GCAGCACTACACTGT | 1108 |
| rs190431482 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CHD4 | GRCh38.p7 | 12:6572364 | CCAGGAGGCAGAGGT[G/T]GTGGTGGGCCAAGAT | 1108 |
| rs190552454 | snp | C/T | 0.110167 | 0.207236 | intron-variant | CHD4 | GRCh38.p7 | 12:6579097 | CAGCAGGCAGATCAC[C/T]TGAGGTCAGGAGTTC | 1108 |
| rs190616390 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | CHD4 | GRCh38.p7 | 12:6599593 | CATCAACTCCTCAGT[A/T]TGAAGTTAGTCCTAT | 1108 |
| rs190658916 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHD4 | GRCh38.p7 | 12:6601863 | TAACAGAGTTAAGAG[A/G]AAAAGAAGAGAAAGT | 1108 |
| rs190683812 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6573784 | ATCCCAGCACTTTGG[C/G]AGGCTGAGGCGGGCA | 1108 |
| rs190731845 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6589196 | GTAAAAAAGAAAGAA[C/T]GTCAGAATATAAAAC | 1108 |
| rs190774344 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CHD4 | GRCh38.p7 | 12:6604626 | TGGAAGTGGAGACAA[A/G]GACAACCCATGGAGG | 1108 |
| rs191027722 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6595054 | CAGATTCCTATGTAA[A/G]TGCATAAAAGCTAGG | 1108 |
| rs191098168 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6575309 | AAAAATTAGTCAGGC[A/G]TGGTGGTACATGCCT | 1108 |
| rs191104299 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | CHD4 | GRCh38.p7 | 12:6595267 | TACTTAAGAGTACCA[A/T]CATTAGACTGCAGCA | 1108 |
| rs191257231 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6574272 | ACTCTTATGTTGTAT[G/T]CACATGAATTTTGTT | 1108 |
| rs191278045 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHD4 | GRCh38.p7 | 12:6578291 | GAACCCACTATCAGT[C/T]TGGCATTCCCTCATC | 1108 |
| rs191400441 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6586784 | CTCATTGCAACCTCC[A/G]CCTCCTGGGTTCAAG | 1108 |
| rs191458955 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant, upstream-variant-2KB | CHD4 | GRCh38.p7 | 12:6606464 | TCACTGTGCGGGGGA[C/G]GGGGGAGAAACACAG | 1108 |
| rs191484882 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CHD4 | GRCh38.p7 | 12:6584879 | ACTGCCACTGAAAGG[A/C]ATGTGAGCATTCTAT | 1108 |
| rs191500895 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6605078 | AACACTAACCCCTCT[C/T]CTAAATGGCCTCAGG | 1108 |
| rs191516710 | snp | A/G | 4.95201e-05 | 0.0049757 | intron-variant | CHD4 | GRCh38.p7 | 12:6598113 | AGCTTTGAGCGGAAA[A/G]AGAAAATCAGCCACC | 1108 |
| rs191796766 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CHD4 | GRCh38.p7 | 12:6600116 | CCAAAGCTCACAACC[A/C]GCAGCACCAGCATTT | 1108 |
| rs191866416 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHD4 | GRCh38.p7 | 12:6592125 | AATAATGCAGTGCCA[A/G]CAACTGAGATCTTTC | 1108 |
| rs192058128 | snp | C/T | 3.29468e-05 | 0.00405861 | missense | CHD4 | GRCh38.p7 | 12:6601739 | CCATGCCCCAGTCTT[C/T]CAGGAGCTGAGCAGA | 1108 |
| rs192133393 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6579811 | CCTGTAATCCCCGCA[C/T]TTTGGGAGGCCAAAG | 1108 |
| rs192316870 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6575635 | ACACCTCATGATTAT[A/T]TGACAGTTTTATAAT | 1108 |
| rs192359317 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CHD4 | GRCh38.p7 | 12:6604026 | CTCATGCCTGTAATC[A/G]CAGCACTCTGGGAGG | 1108 |
| rs192362510 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CHD4 | GRCh38.p7 | 12:6571600 | GGAGGCCAAGGCAGG[C/T]GGGTCACCTGAGGTC | 1108 |
| rs192366569 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CHD4 | GRCh38.p7 | 12:6591028 | CTTGGGAGGCTGAGG[C/T]AGGAGAACTGCTTGA | 1108 |
| rs192609002 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | CHD4 | GRCh38.p7 | 12:6596937 | GCACTCCAGGCTGGG[A/C]CACAGAGCAAGACTC | 1108 |
| rs192676875 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CHD4 | GRCh38.p7 | 12:6595617 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 1108 |
| rs192769055 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CHD4 | GRCh38.p7 | 12:6580339 | TCTTCAGTGTGTCGC[C/T]TCCTCCTGATATCTC | 1108 |
| rs192853647 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6576487 | AACTGGCTAATTTTT[C/G]TATTTTTTGTAGACA | 1108 |
| rs192895387 | snp | A/G | | | upstream-variant-2KB, utr-variant-3-prime | NOP2, CHD4 | GRCh38.p7 | 12:6570220 | GCCGCTGGGTTCCTG[A/G]TATTAAAAAGATGCC | 1108 |
| rs192978513 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHD4 | GRCh38.p7 | 12:6600455 | CTCCCCCCACCCCCC[A/G]ACCCCTATCTCCTTA | 1108 |
| rs192980672 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CHD4 | GRCh38.p7 | 12:6572150 | AAAGGTGGCCAGGGC[A/G]GAGCACAGTGGCTCA | 1108 |
| rs193052312 | snp | C/T | 1.64991e-05 | 0.00287215 | intron-variant | CHD4 | GRCh38.p7 | 12:6602522 | TTTGGCAAAGAGTGG[C/T]AGGCAGGGAAAAGAT | 1108 |
| rs193136496 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CHD4 | GRCh38.p7 | 12:6586148 | TCACGCCTGTAATCC[A/C]AGCACTTTGGGAGGC | 1108 |
| rs193148573 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CHD4 | GRCh38.p7 | 12:6590575 | TATAATCTCAATACT[C/T]TGGGAGGCCAAGGCA | 1108 |
| rs193226938 | snp | C/T | 1.64727e-05 | 0.00286986 | missense, downstream-variant-500B | CHD4, SCARNA11 | GRCh38.p7 | 12:6581095 | CCTTCACCTCTGCCT[C/T]TTCCACTTTCTCCTC | 1108 |
| rs193289474 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | CHD4 | GRCh38.p7 | 12:6605893 | TAGCACAGATGCCCG[C/G]CTGGTCTTTCAAACA | 1108 |
| rs199539910 | snp | C/G | 4.95029e-05 | 0.00497484 | intron-variant | CHD4 | GRCh38.p7 | 12:6570865 | AAGAAGAAAATGGTC[C/G]TACCTGCTGTGGGGT | 1108 |
| rs199553704 | snp | A/G | 0.000346583 | 0.0131595 | synonymous-codon | CHD4 | GRCh38.p7 | 12:6594498 | GACTGCTGTCTGTAC[A/G]GTTTTCCCAAGGCCC | 1108 |
| rs199575698 | snp | C/T | 0.00299557 | 0.0385851 | missense | CHD4 | GRCh38.p7 | 12:6593168 | AGCCCAAAATAGCCA[C/T]GTCAATGGTGATCAA | 1108 |
| rs199588214 | snp | A/T | | | intron-variant | CHD4 | GRCh38.p7 | 12:6599553 | AAGAACATTGCTTCA[A/T]CTCCTCTTAAGAGAG | 1108 |
| rs199652660 | snp | C/T | 0.00199792 | 0.0315431 | synonymous-codon | CHD4 | GRCh38.p7 | 12:6578461 | TTGTTTAATATTTTT[C/T]TTCTGTTTCTCATCA | 1108 |
| rs199660337 | in-del | -/C | | | intron-variant | CHD4 | GRCh38.p7 | 12:6585802 | TCAAAAAAAAAAAAA[-/C]ACACACACAAAGAGG | 1108 |
| rs199667187 | snp | A/G | 0.00102382 | 0.0226023 | intron-variant | CHD4 | GRCh38.p7 | 12:6591439 | CAAATGAGGATTCCT[A/G]AAACTAAACAACTCC | 1108 |
| rs199705744 | snp | A/G | 3.30595e-05 | 0.00406554 | synonymous-codon | CHD4 | GRCh38.p7 | 12:6600598 | ACGGCTGGTGGAACC[A/G]TCAGAAACAGAATAG | 1108 |
| rs199765864 | in-del | -/CA | | | intron-variant | CHD4 | GRCh38.p7 | 12:6580519 | GGAGACTGGCCTGAC[-/CA]ATATGGAGAAACCCC | 1108 |
| rs199773470 | snp | A/C/T | 8.23792e-05 | 0.00641748 | splice-acceptor-variant, downstream-variant-500B | CHD4, SCARNA11 | GRCh38.p7 | 12:6581174 | AGGGGCCTGTGTACA[A/C/T]TTCAAAGGAAAAAAA | 1108 |
| rs199787127 | in-del | -/A | | | intron-variant | CHD4 | GRCh38.p7 | 12:6580829 | CTGGCCAACATGGTG[-/A]AACCCTGTCTCTACT | 1108 |
| rs199795388 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6601587 | ATAAAAAAAGAAAGA[A/G]AAGTAAGAAGAGAGA | 1108 |
| rs199827281 | snp | C/T | 1.65037e-05 | 0.00287256 | missense | CHD4 | GRCh38.p7 | 12:6592463 | TCTTGAACACATCGG[C/T]TTTGAGCCGCCGCAA | 1108 |
| rs199902981 | snp | A/G | | | intron-variant | CHD4 | GRCh38.p7 | 12:6572194 | AGCACTTTGGGAGGC[A/G]GAGGCGGGTGGATCA | 1108 |
| rs199908026 | snp | A/G | 0.000348753 | 0.0132006 | intron-variant | CHD4 | GRCh38.p7 | 12:6600700 | AGAATAAGGTTAGAC[A/G]TTCAAGCCAAGGGGA | 1108 |
| rs199972843 | in-del | -/AA | 0.0349115 | 0.127424 | intron-variant | CHD4 | GRCh38.p7 | 12:6571943 | TCCAGCCTGGGCAAC[-/AA]GAGCAAAACTCCATC | 1108 |
| rs200017158 | snp | A/G | 8.99337e-05 | 0.00670513 | missense, upstream-variant-2KB | CHD4, SCARNA11 | GRCh38.p7 | 12:6581787 | CAGGCATGCTCCAGC[A/G]CCCATTAACATGTTC | 1108 |
| rs200017754 | snp | A/G | 1.64825e-05 | 0.00287071 | intron-variant, nc-transcript-variant | CHD4, SCARNA11 | GRCh38.p7 | 12:6581600 | GGAGCAGAAAAATAG[A/G]CCAGGACAAAAAGAG | 1108 |
| rs200095004 | snp | C/T | 0.000429177 | 0.0146426 | intron-variant | CHD4 | GRCh38.p7 | 12:6597858 | AGCAGGACTCTCCCA[C/T]GGAGACTGCCCGTCT | 1108 |
| rs200098896 | snp | C/G/T | 9.88898e-05 | 0.00703108 | intron-variant | CHD4 | GRCh38.p7 | 12:6573040 | TCAGATCAGGGAGGC[C/G/T]GAATCGGCAGGAGGC | 1108 |
| rs200100295 | snp | A/G/T | 4.95105e-05 | 0.00497526 | synonymous-codon | CHD4 | GRCh38.p7 | 12:6601524 | ATTTTTGGCAGCAAT[A/G/T]AGGGGTCTGGTGGAG | 1108 |
| rs200114730 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | CHD4, SCARNA11 | GRCh38.p7 | 12:6582532 | GCCCACTTCCCTGCA[C/T]GGCTAGGCCTAGAAC | 1108 |
| rs200155885 | snp | C/T | | | intron-variant | CHD4 | GRCh38.p7 | 12:6595972 | AAAAAAAAAAAAAAA[C/T]AAACAACTCTATGCC | 1108 |
| rs200226716 | snp | C/T | 0.000105613 | 0.00726605 | intron-variant, upstream-variant-2KB | CHD4, SCARNA11 | GRCh38.p7 | 12:6582598 | TCTAGATCAGTCCAC[C/T]CCAGCCCTCAACTCA | 1108 |
| rs200229929 | in-del | -/CGCAG | | | upstream-variant-2KB | CHD4 | GRCh38.p7 | 12:6607591 | TGGCCACGCCCCCTT[-/CGCAG]CGGGCGCGCGCGCGT | 1108 |
| rs200253186 | snp | A/G | 1.64806e-05 | 0.00287054 | missense | CHD4 | GRCh38.p7 | 12:6601369 | TCAGTGGCTGTCACC[A/G]TGCTCTCCACCACAG | 1108 |
| rs200285314 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | CHD4 | GRCh38.p7 | 12:6594429 | CACAAAACACCCACA[A/C]AAAAAACTATCCACC | 1108 |
| rs200298091 | in-del | -/C | 0.00255701 | 0.0356646 | intron-variant, downstream-variant-500B | CHD4, SCARNA11 | GRCh38.p7 | 12:6581020 | AAACAAACAAACAAA[-/C]AAAAAAAATGTGGAT | 1108 |
| rs200301256 | snp | C/T | | | intron-variant | CHD4 | GRCh38.p7 | 12:6595558 | TTTGGGAGGCTGAGA[C/T]GGGCGGATCACCTGA | 1108 |
| rs200352853 | snp | A/G | 0.00199792 | 0.0315431 | synonymous-codon | CHD4 | GRCh38.p7 | 12:6573162 | CAAACACTCCACCTC[A/G]GCAAAGCGGGTGTTG | 1108 |
| rs200362476 | snp | C/T | 0.000354069 | 0.0133007 | intron-variant | CHD4 | GRCh38.p7 | 12:6571057 | GAGAAAAAGAGGTGG[C/T]GAGCTGTGGTGGCCC | 1108 |
| rs200373551 | snp | A/C/G | 6.59037e-05 | 0.00574004 | intron-variant | CHD4 | GRCh38.p7 | 12:6591650 | CCTTAGGTCACTAAG[A/C/G]GTTGTCTATGACTGT | 1108 |
| rs200416968 | snp | A/G | 1.65269e-05 | 0.00287457 | intron-variant | CHD4 | GRCh38.p7 | 12:6578017 | CTCAGTACAGATTCA[A/G]GCAAAGGATACTTTA | 1108 |
| rs200434455 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon | CHD4 | GRCh38.p7 | 12:6602134 | CACAAACTCTGGCCC[C/T]TCCCCAGAGCTGTCC | 1108 |
| rs200446221 | in-del | -/ACAACAAC | 0.211819 | 0.247067 | intron-variant | CHD4 | GRCh38.p7 | 12:6580231 | GACTCCATCTCGAAA[-/ACAACAAC]AACAACAACAACAAC | 1108 |
| rs200457661 | snp | A/C/T | 0.000231613 | 0.010759 | intron-variant | CHD4 | GRCh38.p7 | 12:6593073 | TGGGGGCTCCAACAT[A/C/T]CCTCCCTCAGCCCTC | 1108 |
| rs200464782 | snp | A/G | 0.00199804 | 0.031544 | intron-variant | CHD4 | GRCh38.p7 | 12:6601590 | AAAAAAGAAAGAGAA[A/G]TAAGAAGAGAGAACA | 1108 |
| rs200487362 | in-del | -/T | | | intron-variant | CHD4 | GRCh38.p7 | 12:6579069 | CCTGTAATCCCAGCA[-/T]CTTGGGAGACAGCAG | 1108 |
| rs200530735 | snp | A/T | | | missense, downstream-variant-500B | CHD4, SCARNA11 | GRCh38.p7 | 12:6581170 | GGGCAGGGGCCTGTG[A/T]ACACTTCAAAGGAAA | 1108 |
| rs200556426 | snp | C/T | 8.23744e-05 | 0.0064172 | intron-variant | CHD4 | GRCh38.p7 | 12:6602330 | CCCTTCTCAGAGCTC[C/T]TCCCTTCTTCCTCTG | 1108 |
| rs200573419 | snp | A/C | 1.66073e-05 | 0.00288156 | intron-variant | CHD4 | GRCh38.p7 | 12:6593371 | GGTAAACTAAGCCAG[A/C]AGCCACAACTCTTTC | 1108 |
| rs200592113 | snp | C/G | 0.000165303 | 0.00908978 | intron-variant, upstream-variant-2KB | CHD4, SCARNA11 | GRCh38.p7 | 12:6581633 | GGACAGAAAATGATA[C/G]GACAGGCAGACTTAC | 1108 |
| rs200609075 | in-del | -/A/AAAAA/AAAC | 0.263278 | 0.249647 | intron-variant, downstream-variant-500B | CHD4, SCARNA11 | GRCh38.p7 | 12:6581020 | AACAAACAAACAAAC[-/A/AAAAA/AAAC]AAAAAAAATGTGGAT | 1108 |
| rs200652749 | snp | C/T | 0.000535421 | 0.0163531 | intron-variant | CHD4 | GRCh38.p7 | 12:6601240 | ATGCTGTCTTTGACA[C/T]CTTAAGCCCACACTA | 1108 |
| rs200657308 | snp | A/G | 0.000131913 | 0.00812029 | synonymous-codon | CHD4 | GRCh38.p7 | 12:6596119 | GATCAAGTAGTGGAC[A/G]TGGCCCTTCTTGTCC | 1108 |
| rs200660189 | in-del | -/AC | | | intron-variant | CHD4 | GRCh38.p7 | 12:6579598 | ATCTCAAAAAAAAAA[-/AC]AAAACAACAACAAAA | 1108 |
| rs200698074 | snp | C/G | 0.000362528 | 0.0134585 | intron-variant, downstream-variant-500B | CHD4, SCARNA11 | GRCh38.p7 | 12:6581431 | AGGAAGAAGGTACTA[C/G]ATCAGAGAGAAGGTC | 1108 |
| rs200731306 | snp | A/G | 4.94637e-05 | 0.00497287 | synonymous-codon | CHD4 | GRCh38.p7 | 12:6597980 | CTCTGCAAATTTAGG[A/G]TCCTTGTTCTTTCGC | 1108 |
| rs200736113 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6591680 | TTCCCTAAAGCTCCC[A/C]GTCCACATGATACCT | 1108 |
| rs200783211 | snp | C/T | 0.00199803 | 0.031544 | missense | CHD4 | GRCh38.p7 | 12:6578504 | GGGGTCTCTCCATTC[C/T]GAAGCATCACCTCTT | 1108 |
| rs200831097 | snp | C/T | 0.000149208 | 0.00863607 | intron-variant | CHD4 | GRCh38.p7 | 12:6602187 | TACGCTGGAGCAGGG[C/T]AAGGGGGGAAGAGGG | 1108 |
| rs200862176 | in-del | -/T | | | intron-variant | CHD4 | GRCh38.p7 | 12:6580520 | AGACTGGCCTGACCA[-/T]ATATGGAGAAACCCC | 1108 |
| rs200913009 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6593257 | CAACTTGGTCACTAC[C/T]AGTCAGTTCCTCTGT | 1108 |
| rs200931842 | snp | A/G | 0.000164861 | 0.00907764 | intron-variant | CHD4 | GRCh38.p7 | 12:6573041 | CAGATCAGGGAGGCC[A/G]AATCGGCAGGAGGCA | 1108 |
| rs200950618 | snp | A/C/G | 1.70423e-05 | 0.00291905 | intron-variant, upstream-variant-2KB, synonymous-codon | CHD4, SCARNA11 | GRCh38.p7 | 12:6583139 | AGAGGGCAGATGAGC[A/C/G]GGGCCCACTGCTCTA | 1108 |
| rs200953903 | snp | A/G | 0.00199792 | 0.0315431 | synonymous-codon | CHD4 | GRCh38.p7 | 12:6600355 | GCAATAGTCCTGGTG[A/G]TCTGTCTCATAACCA | 1108 |
| rs201011723 | snp | A/G | 0.000445005 | 0.0149099 | intron-variant | CHD4 | GRCh38.p7 | 12:6577920 | GGCATAGCCATGGCT[A/G]TTGGAAAAGTGCTCA | 1108 |
| rs201047688 | snp | C/G | 0.000947938 | 0.0217502 | missense | CHD4 | GRCh38.p7 | 12:6578526 | TCACCTCTTTTTTCT[C/G]TTCTTCTTCTTTCTT | 1108 |
| rs201056205 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHD4 | GRCh38.p7 | 12:6580303 | GGGAAAACCTGCCAC[C/T]TAAAATCAAGGGTGC | 1108 |
| rs201057993 | in-del | -/TT | | | upstream-variant-2KB, utr-variant-3-prime | NOP2, CHD4 | GRCh38.p7 | 12:6570158 | CCTTTTTTTTTTTTT[-/TT]CCACTTTATTTCATT | 1108 |
| rs201070575 | snp | C/T | 0.000132542 | 0.00813964 | synonymous-codon | CHD4 | GRCh38.p7 | 12:6593181 | CATGTCAATGGTGAT[C/T]AATTCATAGGATGTC | 1108 |
| rs201121936 | snp | A/C | 1.64746e-05 | 0.00287002 | missense | CHD4 | GRCh38.p7 | 12:6570921 | CGGCTGAGAATGTTA[A/C]GCTCTGACATCTGTA | 1108 |
| rs201167959 | snp | C/T | 0.000347714 | 0.0131809 | intron-variant | CHD4 | GRCh38.p7 | 12:6598213 | ATCTCCAGACTATCC[C/T]AAACTTACCTGCAGT | 1108 |
| rs201176021 | snp | C/T | 0.00199808 | 0.0315444 | intron-variant | CHD4 | GRCh38.p7 | 12:6599737 | GAAAAGACTACACTT[C/T]CCCATTTTTTGCCCC | 1108 |
| rs201224992 | snp | A/G | 0.000115334 | 0.00759299 | missense | CHD4 | GRCh38.p7 | 12:6595347 | ACATCAACTGTTGGC[A/G]TTTCTGGAGGCCTCT | 1108 |
| rs201237481 | in-del | -/A | 0.0123036 | 0.0774623 | intron-variant | CHD4 | GRCh38.p7 | 12:6583697 | AAAGATAGCAAAAAG[-/A]AAAGAGGTCAGAGCC | 1108 |
| rs201292229 | snp | A/G | 0.00153682 | 0.0276776 | intron-variant | CHD4 | GRCh38.p7 | 12:6593666 | CCCCAGCACACTGCA[A/G]CCCCAGCGAACACCC | 1108 |
| rs201313750 | snp | A/C | 0.0011527 | 0.0239796 | intron-variant | CHD4 | GRCh38.p7 | 12:6591833 | GGAGCTTCCTGAGAA[A/C]AAATGCAAAGAAAAA | 1108 |
| rs201328163 | in-del | -/C | | | upstream-variant-2KB | CHD4 | GRCh38.p7 | 12:6607597 | GCCCCCTTCGCAGCG[-/C]GGCGCGCGCGCGTCA | 1108 |
| rs201353338 | snp | A/G | 0.000181265 | 0.0095184 | synonymous-codon | CHD4 | GRCh38.p7 | 12:6597911 | GTGGTTGAGGATTCG[A/G]TGGATCATCATCCAC | 1108 |
| rs201417262 | snp | A/G | | | stop-gained, downstream-variant-500B | CHD4, SCARNA11 | GRCh38.p7 | 12:6581167 | CAGGGGCAGGGGCCT[A/G]TGTACACTTCAAAGG | 1108 |
| rs201440607 | snp | A/G | 1.66217e-05 | 0.0028828 | missense, intron-variant | CHD4 | GRCh38.p7 | 12:6602160 | TGTCCCCCAGCTGCC[A/G]GCATAAGAGCATACG | 1108 |
| rs201471909 | snp | A/C/T | 9.88328e-05 | 0.00702906 | missense, downstream-variant-500B | CHD4, SCARNA11 | GRCh38.p7 | 12:6581143 | CAACGACCTTTTCAT[A/C/T]CTCTGAGGCAGGGGC | 1108 |
| rs201490082 | snp | A/G | 0.000313834 | 0.0125227 | synonymous-codon, upstream-variant-2KB | CHD4, SCARNA11 | GRCh38.p7 | 12:6582662 | TCTTACAAGCCACTG[A/G]GTAGTAAAAGCATCC | 1108 |
| rs201534121 | snp | A/C | 0.0420626 | 0.138788 | missense | CHD4 | GRCh38.p7 | 12:6600591 | GGCTACTACGGCTGG[A/C]GGAACCATCAGAAAC | 1108 |
| rs201539057 | in-del | -/ACAACAAC | | | intron-variant | CHD4 | GRCh38.p7 | 12:6580234 | TCCATCTCGAAAACA[-/ACAACAAC]AACAACAACAACAAC | 1108 |
| rs201602922 | in-del | -/A | | | intron-variant | CHD4 | GRCh38.p7 | 12:6575450 | GTAAGACTTTGTCTC[-/A]AAAAAAAAAAAAAAA | 1108 |
| rs201605768 | snp | G/T | 0.000280244 | 0.011834 | intron-variant | CHD4 | GRCh38.p7 | 12:6591622 | TATGGAAGAGTCAGA[G/T]GGTAATCCCTTTCCT | 1108 |
| rs201625860 | in-del | -/CCT | | | cds-indel | CHD4 | GRCh38.p7 | 12:6602000 | CCTCCTCCTCCTCCT[-/CCT]TCCGCTTGGATTTGC | 1108 |
| rs201636143 | snp | C/G | 0.00051246 | 0.015999 | intron-variant | CHD4 | GRCh38.p7 | 12:6596149 | CACACTGCAAGTCCA[C/G]GAGAGAAAACCCTCA | 1108 |
| rs201646319 | snp | C/T | 0.000115419 | 0.00759581 | intron-variant | CHD4 | GRCh38.p7 | 12:6598147 | AAGCTGTGTTCATTC[C/T]TTCTATCCACAAGGC | 1108 |
| rs201703851 | snp | G/T | 4.95021e-05 | 0.0049748 | intron-variant | CHD4 | GRCh38.p7 | 12:6597860 | CAGGACTCTCCCACG[G/T]AGACTGCCCGTCTCC | 1108 |
| rs201711195 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6600693 | ATGAAAAAGAATAAG[C/G]TTAGACGTTCAAGCC | 1108 |
| rs201713210 | snp | A/C | | | upstream-variant-2KB | CHD4 | GRCh38.p7 | 12:6608051 | AGAAACTCACCCCCC[A/C]CCATACTACAACAAC | 1108 |
| rs201738406 | snp | C/T | 0.00199792 | 0.0315431 | missense | CHD4 | GRCh38.p7 | 12:6597999 | TTGTTCTTTCGCTTT[C/T]GGCTTTTCTCTTCAT | 1108 |
| rs201751048 | snp | A/G | 0.00316168 | 0.0396339 | synonymous-codon | CHD4 | GRCh38.p7 | 12:6573102 | TGCATTGGCTGGCTT[A/G]TTTCCTGCCATTGAC | 1108 |
| rs201755804 | snp | A/G | 0.000132018 | 0.00812351 | intron-variant | CHD4 | GRCh38.p7 | 12:6601559 | GCACAAGAGCAGAGG[A/G]AAAGGTTTAAGAATA | 1108 |
| rs201795544 | snp | C/T | 8.9328e-05 | 0.00668252 | intron-variant | CHD4 | GRCh38.p7 | 12:6600900 | AGACATGGCACCCTC[C/T]CTAAAGCGATGGGCT | 1108 |
| rs201854884 | snp | A/T | 0.000939764 | 0.0216564 | intron-variant | CHD4 | GRCh38.p7 | 12:6602502 | CTCTTCATTTTCTAC[A/T]TATATTTGGCAAAGA | 1108 |
| rs201933013 | snp | A/G | 3.34146e-05 | 0.00408732 | intron-variant | CHD4 | GRCh38.p7 | 12:6578961 | ACCTAAAGGAAGAAC[A/G]TTCTCCTCTGTTGCA | 1108 |
| rs201942144 | snp | A/G | 0.000428301 | 0.0146276 | intron-variant, downstream-variant-500B | CHD4, SCARNA11 | GRCh38.p7 | 12:6581266 | ATTTGTCTTTAGTAT[A/G]GCATTCAGTCACCCC | 1108 |
| rs201992075 | snp | C/T | 0.000131774 | 0.00811601 | missense, downstream-variant-500B | CHD4, SCARNA11 | GRCh38.p7 | 12:6581131 | CAGGGGGTTCAACAA[C/T]GACCTTTTCATCCTC | 1108 |
| rs202019064 | snp | A/G | 8.24069e-05 | 0.00641846 | synonymous-codon | CHD4 | GRCh38.p7 | 12:6570887 | CTGTGGGGTAGGTTC[A/G]GGTGCCCGGTTTGCC | 1108 |
| rs202049023 | snp | A/G | 4.95291e-05 | 0.00497615 | intron-variant | CHD4 | GRCh38.p7 | 12:6570851 | GAAGAGGTGGTGTCA[A/G]GAAGAAAATGGTCCT | 1108 |
| rs202095449 | in-del | -/G | | | intron-variant | CHD4 | GRCh38.p7 | 12:6579072 | TAATCCCAGCATCTT[-/G]GGGAGACAGCAGCAG | 1108 |
| rs202131693 | snp | C/T | 1.7505e-05 | 0.00295841 | intron-variant, upstream-variant-2KB | CHD4, SCARNA11 | GRCh38.p7 | 12:6582604 | TCAGTCCACTCCAGC[C/T]CTCAACTCACTTGAA | 1108 |
| rs202139891 | snp | A/C/G | 8.32042e-05 | 0.0064495 | missense, synonymous-codon | CHD4 | GRCh38.p7 | 12:6602146 | CCCCTCCCCAGAGCT[A/C/G]TCCCCCAGCTGCCGG | 1108 |
| rs202233858 | snp | A/G | 3.29826e-05 | 0.00406082 | missense | CHD4 | GRCh38.p7 | 12:6592793 | GCTTGTGCTGGAGTG[A/G]GTAACCATTCAATAC | 1108 |
| rs207472635 | snp | A/G | | | intron-variant | CHD4 | GRCh38.p7 | 12:6573380 | GTAATAAGAACCTAT[A/G]AAGAACTTCATGGAC | 1108 |
| rs267603638 | snp | A/G | | | missense | CHD4 | GRCh38.p7 | 12:6600945 | GATCTCTTACGCTTG[A/G]AACCAAAACCTCCCA | 1108 |
| rs367601246 | snp | A/C/G | 0.000115405 | 0.00759548 | intron-variant | CHD4 | GRCh38.p7 | 12:6587691 | GCCCCACACCAAAAC[A/C/G]TAAGTTCCTGACTAC | 1108 |
| rs367728804 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CHD4 | GRCh38.p7 | 12:6596605 | GGGAGTTCAAGACCA[A/G]TCTGGCCAGCATGGA | 1108 |
| rs367790494 | snp | A/G/T | 9.89511e-05 | 0.00703319 | intron-variant | CHD4 | GRCh38.p7 | 12:6577942 | AAGTGCTCAGGAAAA[A/G/T]CAAAACAAGGAAAGT | 1108 |
| rs367917436 | snp | C/T | | | intron-variant | CHD4 | GRCh38.p7 | 12:6577327 | CTCAGGAGGCTGAGG[C/T]GGGAGAATCACTTAA | 1108 |
| rs367953962 | snp | A/G | 9.90606e-05 | 0.00703708 | intron-variant | CHD4 | GRCh38.p7 | 12:6587610 | GTTTCAGCAGCTGCA[A/G]TGGAAAAAGCAAGTC | 1108 |
| rs368003608 | snp | A/G | 3.29549e-05 | 0.00405911 | synonymous-codon | CHD4 | GRCh38.p7 | 12:6594588 | GCCCTCCATTTGATA[A/G]GGGTGCAGGGTTCCA | 1108 |
| rs368025848 | snp | C/G | 1.64768e-05 | 0.00287021 | intron-variant | CHD4 | GRCh38.p7 | 12:6591656 | GTCACTAAGGGTTGT[C/G]TATGACTGTTCCCTA | 1108 |
| rs368067995 | snp | C/G | 3.51056e-05 | 0.00418946 | intron-variant | CHD4 | GRCh38.p7 | 12:6601061 | ATTGGGACCTAAAAT[C/G]AGGATATATCCAAAT | 1108 |
| rs368097200 | snp | C/T | 1.66793e-05 | 0.0028878 | synonymous-codon | CHD4 | GRCh38.p7 | 12:6573252 | CTGTTCCTCAATCAC[C/T]AGAGCTTGTTCTAAG | 1108 |
| rs368112823 | snp | A/G | 1.73249e-05 | 0.00294315 | synonymous-codon | CHD4 | GRCh38.p7 | 12:6602008 | CTCCTCCTTCCGCTT[A/G]GATTTGCTCTTCTTC | 1108 |
| rs368117224 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6585933 | TGAAACCCCGTTTCT[A/C]CTAAAACTATAAAAA | 1108 |
| rs368125487 | snp | C/T | | | intron-variant | CHD4 | GRCh38.p7 | 12:6595701 | ACTGAGGCAGGAGAA[C/T]TGCTTGAACCCAGGA | 1108 |
| rs368227033 | snp | A/C | 0.000437904 | 0.0147905 | utr-variant-3-prime | CHD4 | GRCh38.p7 | 12:6570620 | GGGAGAAGCTGGGAC[A/C]AGAGAAAGTGAGGAA | 1108 |
| rs368236345 | snp | G/T | 0.000153988 | 0.00877328 | missense | CHD4 | GRCh38.p7 | 12:6601345 | ACAGGGGGAGGTGGT[G/T]GTGCAACCTCAGTGG | 1108 |
| rs368239388 | snp | A/C/G | 9.88605e-05 | 0.00703004 | intron-variant | CHD4 | GRCh38.p7 | 12:6591860 | AAAAAGTATTAAAAG[A/C/G]AAGCCCACATGGAGA | 1108 |
| rs368241764 | snp | C/G | 1.66432e-05 | 0.00288467 | intron-variant | CHD4 | GRCh38.p7 | 12:6596182 | GCCAGAAAAGGCAAC[C/G]CTCCTCACTTCCTCT | 1108 |
| rs368247943 | snp | A/G | 3.30049e-05 | 0.00406219 | intron-variant | CHD4 | GRCh38.p7 | 12:6577735 | GCTGCAGGACGTTAC[A/G]CACTTTCAAGTTTGT | 1108 |
| rs368306542 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CHD4 | GRCh38.p7 | 12:6588971 | TGTCAGAATAGGCCA[C/G]GTGCAGTGACTCACA | 1108 |
| rs368436665 | snp | A/G | 1.80393e-05 | 0.00300322 | synonymous-codon, upstream-variant-2KB | CHD4, SCARNA11 | GRCh38.p7 | 12:6581797 | CCAGCGCCCATTAAC[A/G]TGTTCAAACTCCTGA | 1108 |
| rs368491094 | snp | A/G | 6.59131e-05 | 0.0057404 | intron-variant | CHD4 | GRCh38.p7 | 12:6577779 | TATTCCTCCCCAACC[A/G]CTCACCTTAAACCTT | 1108 |
| rs368535172 | in-del | -/ATC | | | intron-variant | CHD4 | GRCh38.p7 | 12:6589484 | TGAAAAGGACACATC[-/ATC]GACTGGGCGTGGTGG | 1108 |
| rs368599010 | snp | C/T | | | intron-variant | CHD4 | GRCh38.p7 | 12:6605644 | CCTTCTTTTGCCCCT[C/T]TTCACTAGGCTATTA | 1108 |
| rs368689531 | snp | A/G | 1.66463e-05 | 0.00288494 | missense | CHD4 | GRCh38.p7 | 12:6578132 | TCTGCCAAAGGGAGT[A/G]CAACTCTGAGGAGGA | 1108 |
| rs368719400 | snp | A/T | 3.31252e-05 | 0.00406958 | intron-variant | CHD4 | GRCh38.p7 | 12:6578928 | AGCACCTAGGGGAAG[A/T]AATGTTATTGAGACT | 1108 |
| rs368737019 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6585334 | CTGTCCCCCAGGCTG[A/G]AGTGCAGTGGGGCAA | 1108 |
| rs368788369 | snp | C/T | 1.79149e-05 | 0.00299285 | intron-variant | CHD4 | GRCh38.p7 | 12:6601097 | CCACAAGACCAAAGA[C/T]GGGGAAAATAAAATC | 1108 |
| rs368833592 | snp | A/C | 6.60818e-05 | 0.00574774 | intron-variant | CHD4 | GRCh38.p7 | 12:6599749 | CTTTCCCATTTTTTG[A/C]CCCGGCTGAGATCAG | 1108 |
| rs368852616 | snp | A/G | | | intron-variant, upstream-variant-2KB | CHD4 | GRCh38.p7 | 12:6607081 | GAGACCAAGCCGGAG[A/G]CGGGGGGTCGCGGGG | 1108 |
| rs368884385 | snp | A/G | 6.62844e-05 | 0.00575655 | intron-variant | CHD4 | GRCh38.p7 | 12:6602195 | AGCAGGGCAAGGGGG[A/G]AAGAGGGAGACAGAC | 1108 |
| rs368924391 | snp | C/T | | | synonymous-codon, upstream-variant-2KB | CHD4, SCARNA11 | GRCh38.p7 | 12:6583340 | AGGATCCACACTTTC[C/T]TCCTGTTTAATGATT | 1108 |
| rs368955565 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | CHD4 | GRCh38.p7 | 12:6609103 | TCATGTTCATTCAAC[C/T]TGTGTTGACAGAGTA | 1108 |
| rs368992258 | snp | A/G | 0.000102589 | 0.00716127 | intron-variant | CHD4 | GRCh38.p7 | 12:6600061 | CCCCACCCGCCCACC[A/G]CAGTCTGAAGCCAGT | 1108 |
| rs369023810 | snp | A/G | 1.6477e-05 | 0.00287024 | synonymous-codon | CHD4 | GRCh38.p7 | 12:6570905 | TGCCCGGTTTGCCAG[A/G]CGGCTGAGAATGTTA | 1108 |
| rs369033100 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHD4 | GRCh38.p7 | 12:6574614 | GATGATTTGATGCTT[C/T]TCAAACATGTACCTT | 1108 |
| rs369153089 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon | CHD4 | GRCh38.p7 | 12:6599974 | CTCCTCACCCTCCGA[A/G]TTGTCCTCTTTAGCT | 1108 |
| rs369165349 | snp | A/G | 3.30912e-05 | 0.00406749 | synonymous-codon | CHD4 | GRCh38.p7 | 12:6591467 | TCCTTCTCTCTCACC[A/G]TTGAAGCGGTCAATG | 1108 |
| rs369196306 | snp | C/T | 0.00131314 | 0.0255899 | intron-variant | CHD4 | GRCh38.p7 | 12:6570782 | AGGCCACCCACCCAG[C/T]ATGTAAAGCTAGGGA | 1108 |
| rs369216336 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHD4 | GRCh38.p7 | 12:6605228 | ACAAAAACAGGATCA[A/G]CAGGCTCCAGAATGA | 1108 |
| rs369228909 | snp | A/G | 3.2962e-05 | 0.00405954 | missense | CHD4 | GRCh38.p7 | 12:6597946 | GTTTTATCCCATAGC[A/G]ATAGAAGCGTTCCTC | 1108 |
| rs369248777 | snp | A/G | 0.000131911 | 0.00812022 | intron-variant | CHD4 | GRCh38.p7 | 12:6570733 | AGAATTCCAGATGAT[A/G]GGAATCCACCCAATC | 1108 |
| rs369257422 | snp | C/T | | | intron-variant | CHD4 | GRCh38.p7 | 12:6603164 | CCGAATCAGCCCAGC[C/T]GTCACCATCTCCCCT | 1108 |
| rs369320818 | snp | G/T | 1.65051e-05 | 0.00287267 | intron-variant | CHD4 | GRCh38.p7 | 12:6587606 | GTCAGTTTCAGCAGC[G/T]GCAGTGGAAAAAGCA | 1108 |
| rs369343847 | in-del | -/C | | | upstream-variant-2KB | CHD4 | GRCh38.p7 | 12:6608053 | AACTCACCCCCCCCC[-/C]ATACTACAACAACGG | 1108 |
| rs369442467 | snp | A/C | 0.000153988 | 0.00877328 | intron-variant, upstream-variant-2KB | CHD4, SCARNA11 | GRCh38.p7 | 12:6582114 | GGCCCCCTAGAAACA[A/C]TGGCAAGAGGCTCAG | 1108 |
| rs369530411 | snp | A/G | | | intron-variant | CHD4 | GRCh38.p7 | 12:6585433 | GGACTACAGGCGCCC[A/G]CCACCACGCCCAGCT | 1108 |
| rs369580924 | snp | C/T | | | intron-variant | CHD4 | GRCh38.p7 | 12:6590860 | CTGGGCGTGGTGGCT[C/T]GTGCCTGTAATCCCA | 1108 |
| rs369595705 | snp | A/G | 0.000434892 | 0.0147396 | intron-variant | CHD4 | GRCh38.p7 | 12:6592104 | CTTGAGAGCCTTTCA[A/G]TGACTAATAATGCAG | 1108 |
| rs369600268 | snp | A/G | | | intron-variant | CHD4 | GRCh38.p7 | 12:6573938 | TTGAGGCAGAAGAAT[A/G]CTTGAACCCGGGAGG | 1108 |
| rs369640320 | snp | C/T | 1.65512e-05 | 0.00287669 | intron-variant | CHD4 | GRCh38.p7 | 12:6598183 | TGTCACTATCCTCTT[C/T]ATCGTAGCCCCTACA | 1108 |
| rs369668601 | snp | A/C | 1.66258e-05 | 0.00288316 | intron-variant | CHD4 | GRCh38.p7 | 12:6595987 | GAAACAACTCTATGC[A/C]TCACCCAAAATCACT | 1108 |
| rs369758311 | snp | C/T | 3.48967e-05 | 0.00417698 | intron-variant | CHD4 | GRCh38.p7 | 12:6606228 | AGTCACTCGGGAGAG[C/T]CCCAGATGTCTCCTT | 1108 |
| rs369776883 | snp | C/T | | | intron-variant | CHD4 | GRCh38.p7 | 12:6573395 | GAAGAACTTCATGGA[C/T]AGCTCATTCCCACAC | 1108 |
| rs369840095 | snp | A/G | 0.000116499 | 0.00763124 | intron-variant | CHD4 | GRCh38.p7 | 12:6592609 | TTGGAGAAGGAGAAA[A/G]GAAGAAAGAAAAGTG | 1108 |
| rs369850020 | snp | A/C | | | upstream-variant-2KB | CHD4 | GRCh38.p7 | 12:6607499 | TCAACCAACTCCAAC[A/C]CCCCCCTTCCACTAC | 1108 |
| rs369857098 | snp | C/G | 3.29707e-05 | 0.00406008 | intron-variant | CHD4 | GRCh38.p7 | 12:6570709 | CTAGAGAAGGAGACC[C/G]GAGGAGTCAGAATTC | 1108 |
| rs369950785 | snp | A/G | 1.6483e-05 | 0.00287076 | intron-variant | CHD4 | GRCh38.p7 | 12:6595434 | CTCATTAACTCCCTA[A/G]AGAAGAAAGACATCA | 1108 |
| rs370021329 | snp | A/G | 1.64768e-05 | 0.00287021 | intron-variant, downstream-variant-500B | CHD4, SCARNA11 | GRCh38.p7 | 12:6581391 | TTTATCCCATCTTCT[A/G]CAGAACAATAAAAGA | 1108 |
| rs370021586 | snp | C/G | | | intron-variant | CHD4 | GRCh38.p7 | 12:6585030 | ATCAGGGAAACACAG[C/G]AAGGGGGATGGTTCT | 1108 |
| rs370033438 | snp | A/C | 0.000153988 | 0.00877328 | intron-variant, upstream-variant-2KB | CHD4, SCARNA11 | GRCh38.p7 | 12:6582594 | TTGCTCTAGATCAGT[A/C]CACTCCAGCCCTCAA | 1108 |
| rs370046089 | snp | G/T | | | intron-variant | CHD4 | GRCh38.p7 | 12:6586444 | TACATACACAAGGAG[G/T]CCTGGTGTGGTGGCT | 1108 |
| rs370071477 | snp | A/C/G | 0.000280177 | 0.0118327 | intron-variant | CHD4 | GRCh38.p7 | 12:6595433 | CCTCATTAACTCCCT[A/C/G]AAGAAGAAAGACATC | 1108 |
| rs370159668 | snp | A/G | | | intron-variant | CHD4 | GRCh38.p7 | 12:6579964 | AGGAGGCTGAGGCAG[A/G]AGAATGGTGTGAACC | 1108 |
| rs370190894 | snp | A/G | 1.64757e-05 | 0.00287012 | synonymous-codon | CHD4 | GRCh38.p7 | 12:6593530 | GGTTACGACATACAT[A/G]TCTGGAGCCCACATT | 1108 |
| rs370199052 | snp | A/T | 0.00102098 | 0.0225709 | intron-variant | CHD4 | GRCh38.p7 | 12:6591658 | CACTAAGGGTTGTCT[A/T]TGACTGTTCCCTAAA | 1108 |
| rs370211517 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CHD4 | GRCh38.p7 | 12:6588059 | AAGGTCCACAGCCTA[C/T]ATTCATAGGAAACTT | 1108 |
| rs370214171 | snp | A/C | 1.65021e-05 | 0.00287241 | intron-variant | CHD4 | GRCh38.p7 | 12:6577963 | CAAGGAAAGTAAGAA[A/C]CTCAAACTAAAAGAC | 1108 |
| rs370228207 | snp | C/T | 0.00107433 | 0.0231519 | intron-variant | CHD4 | GRCh38.p7 | 12:6591438 | GCAAATGAGGATTCC[C/T]GAAACTAAACAACTC | 1108 |
| rs370238992 | snp | C/T | | | upstream-variant-2KB | CHD4 | GRCh38.p7 | 12:6608859 | GATGAAACATTTACA[C/T]GAAGTCTAATTCACC | 1108 |
| rs370271547 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CHD4 | GRCh38.p7 | 12:6596522 | GCCAGGCATCAGGCC[A/G]GGCGCGGTGGCTCAC | 1108 |
| rs370333357 | snp | A/G | 1.72782e-05 | 0.00293918 | intron-variant | CHD4 | GRCh38.p7 | 12:6601914 | GTCTAGGAAACAAAA[A/G]GACAAAAGTTTAACA | 1108 |
| rs370369438 | snp | A/G | 0.000171072 | 0.00924698 | synonymous-codon, upstream-variant-2KB | CHD4, SCARNA11 | GRCh38.p7 | 12:6582272 | CCGCATGAAAAGAGA[A/G]ACATATGCCCTGTGT | 1108 |
| rs370385858 | snp | C/T | 3.54881e-05 | 0.00421222 | intron-variant | CHD4 | GRCh38.p7 | 12:6601080 | ATATATCCAAATATA[C/T]ACCACAAGACCAAAG | 1108 |
| rs370395841 | snp | A/G | | | intron-variant | CHD4 | GRCh38.p7 | 12:6592688 | ATTACAGATAAACAC[A/G]TACTTACTGGAACCT | 1108 |
| rs370426958 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6584038 | AAATAAATTACAATC[A/G]GCCCTCTGTATCCAC | 1108 |
| rs370454407 | snp | A/G | | | upstream-variant-2KB | CHD4 | GRCh38.p7 | 12:6609168 | AAGGAAGACCAGGGG[A/G]CCTCCCTTCAAAAAG | 1108 |
| rs370470848 | snp | A/C/G/T | 0.000199001 | 0.00997323 | intron-variant, upstream-variant-2KB, missense | CHD4, SCARNA11 | GRCh38.p7 | 12:6583173 | GAACGGCCCATGGGT[A/C/G/T]GGGGGCGGGGCCGGC | 1108 |
| rs370479507 | snp | A/G/T | 3.51693e-05 | 0.00419329 | intron-variant | CHD4 | GRCh38.p7 | 12:6573285 | CTGGACAAGGGATAA[A/G/T]AGGAAACGGGAGTTC | 1108 |
| rs370585666 | snp | C/T | 6.96718e-05 | 0.00590179 | utr-variant-5-prime | CHD4 | GRCh38.p7 | 12:6606375 | AGGCCCGACGCCATC[C/T]CCTTCCGCTCCCGGC | 1108 |
| rs370600359 | snp | C/G | | | upstream-variant-2KB | CHD4 | GRCh38.p7 | 12:6608176 | TCAGTCCCTGCAGGC[C/G]AGGGTCTAGAGGCTC | 1108 |
| rs370626030 | snp | A/G | 1.64825e-05 | 0.00287071 | synonymous-codon | CHD4 | GRCh38.p7 | 12:6577914 | CCACCGGGCATAGCC[A/G]TGGCTATTGGAAAAG | 1108 |
| rs370653615 | snp | C/T | | | upstream-variant-2KB, downstream-variant-500B | NOP2, CHD4 | GRCh38.p7 | 12:6570014 | CTTAATTTTCAACTA[C/T]ACAGGTGCCAGGCTC | 1108 |
| rs370679311 | snp | A/C/T | 0.000102266 | 0.00715008 | synonymous-codon | CHD4 | GRCh38.p7 | 12:6606290 | TGGGTGGGGTGGGGG[A/C/T]AGGCTGTTGTTCAAA | 1108 |
| rs370820351 | snp | A/C/T | 4.94893e-05 | 0.00497419 | intron-variant | CHD4 | GRCh38.p7 | 12:6587584 | ATCAAGGGCCCACAT[A/C/T]CCCAAAGTCAGTTTC | 1108 |
| rs370822253 | snp | C/G | 8.23608e-05 | 0.00641667 | missense | CHD4 | GRCh38.p7 | 12:6602412 | CTTAGGGATTTTAGG[C/G]TCCCGAGGTTTCTTA | 1108 |
| rs370838776 | snp | A/G | 4.99988e-05 | 0.00499969 | intron-variant | CHD4 | GRCh38.p7 | 12:6592850 | GAAAGGTGAAATCCA[A/G]TGAAAACAGAGCTCT | 1108 |
| rs371006626 | snp | A/C | 0.000164775 | 0.00907525 | intron-variant | CHD4 | GRCh38.p7 | 12:6577777 | TATATTCCTCCCCAA[A/C]CGCTCACCTTAAACC | 1108 |
| rs371021197 | snp | A/G | 0.000307953 | 0.0124049 | intron-variant | CHD4 | GRCh38.p7 | 12:6600911 | CCTCCCTAAAGCGAT[A/G]GGCTGGGCTCTCACC | 1108 |
| rs371027525 | snp | A/G | | | intron-variant | CHD4 | GRCh38.p7 | 12:6571789 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 1108 |
| rs371075410 | snp | A/C | 0.000153988 | 0.00877328 | intron-variant, downstream-variant-500B | CHD4, SCARNA11 | GRCh38.p7 | 12:6581192 | CAAAGGAAAAAAAAA[A/C]AAAAACAAAACAGAT | 1108 |
| rs371205280 | snp | A/G | | | intron-variant | CHD4 | GRCh38.p7 | 12:6575906 | CTGGCTCACATCTTT[A/G]CCCAACCTAATCCCT | 1108 |
| rs371206767 | snp | A/G | 1.65228e-05 | 0.00287422 | synonymous-codon | CHD4 | GRCh38.p7 | 12:6600634 | GATACTGGCATCATC[A/G]AAGTCAGATTCCACA | 1108 |
| rs371206907 | snp | C/G | 1.78048e-05 | 0.00298364 | intron-variant, upstream-variant-2KB | CHD4, SCARNA11 | GRCh38.p7 | 12:6582576 | GATAGATAGCAGAAG[C/G]CCTTGCTCTAGATCA | 1108 |
| rs371228907 | snp | C/T | | | intron-variant | CHD4 | GRCh38.p7 | 12:6598611 | GTCAAGAGATCGAGA[C/T]CATCCTAGCTAACAT | 1108 |
| rs371268726 | snp | C/T | 5.18686e-05 | 0.00509231 | missense | CHD4 | GRCh38.p7 | 12:6602027 | TTGCTCTTCTTCTCT[C/T]TCTTAGGTCCAAGCT | 1108 |
| rs371269383 | snp | A/G | | | intron-variant | CHD4 | GRCh38.p7 | 12:6602918 | CAGAAGGCAAAAACT[A/G]TAGAATATACCTTCC | 1108 |
| rs371270045 | snp | A/T | | | intron-variant | CHD4 | GRCh38.p7 | 12:6604303 | AAATAATATCCCTCC[A/T]TCAATCCCTGACATG | 1108 |
| rs371336037 | snp | C/T | 3.30186e-05 | 0.00406303 | missense | CHD4 | GRCh38.p7 | 12:6598325 | TTTGGGGAGGGCGTG[C/T]TGGGATCAGCATCTG | 1108 |
| rs371393096 | snp | A/G | 0.000296711 | 0.0121765 | intron-variant | CHD4 | GRCh38.p7 | 12:6591614 | GGTTTAATTATGGAA[A/G]AGTCAGATGGTAATC | 1108 |
| rs371406609 | in-del | -/C | | | intron-variant | CHD4 | GRCh38.p7 | 12:6605277 | AGGAATGAAGAAATG[-/C]ACATGTAGAAAAAAA | 1108 |
| rs371408838 | snp | C/T | 0.00011532 | 0.00759255 | synonymous-codon | CHD4 | GRCh38.p7 | 12:6577821 | TTTATTCTTGATCTC[C/T]AAGAAATTGCCACGG | 1108 |
| rs371468099 | snp | C/T | | | intron-variant | CHD4 | GRCh38.p7 | 12:6588817 | GGGAATGGTGGCACA[C/T]GCCTGTAGTCCCAGC | 1108 |
| rs371501457 | snp | G/T | 1.64977e-05 | 0.00287203 | utr-variant-3-prime | CHD4 | GRCh38.p7 | 12:6570633 | ACAAGAGAAAGTGAG[G/T]AAGGTCACTGCTCAG | 1108 |
| rs371614957 | snp | A/G | 4.94556e-05 | 0.00497246 | intron-variant | CHD4 | GRCh38.p7 | 12:6597877 | GACTGCCCGTCTCCC[A/G]TGTGCTCAGCTGGTA | 1108 |
| rs371665146 | snp | A/C | 1.65444e-05 | 0.00287609 | intron-variant | CHD4 | GRCh38.p7 | 12:6595289 | ACTGCAGCAAAGATA[A/C]ATTGTCCTACCCAAC | 1108 |
| rs371667614 | snp | A/G | 8.49365e-05 | 0.00651621 | intron-variant | CHD4 | GRCh38.p7 | 12:6573272 | CTTGTTCTAAGAGCT[A/G]GACAAGGGATAAGAG | 1108 |
| rs371703431 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6572214 | CGGGTGGATCACTTG[A/G]AGTCAGTTTGAGACC | 1108 |
| rs371892773 | snp | A/G | | | intron-variant | CHD4 | GRCh38.p7 | 12:6604465 | AATAAGACCAGGCAC[A/G]AGAACGCCCCTCCCA | 1108 |
| rs371899638 | snp | C/G | | | intron-variant | CHD4 | GRCh38.p7 | 12:6571866 | CTTGGGAAGCTGAGG[C/G]AGGAGAATCGCTTGA | 1108 |
| rs371917637 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | CHD4 | GRCh38.p7 | 12:6602285 | GGCCCACCACTTCTG[A/G]GAAAGAAACAAATGC | 1108 |
| rs371949772 | snp | C/G | 1.64743e-05 | 0.00287 | intron-variant | CHD4 | GRCh38.p7 | 12:6591886 | GGAGAAGACCCAACC[C/G]AGGGAGGAACAGGAG | 1108 |
| rs372030137 | snp | A/T | | | intron-variant | CHD4 | GRCh38.p7 | 12:6573422 | ACACCCAAGTAGTTT[A/T]ACTTTGCCTTGTAAC | 1108 |
| rs372040899 | snp | C/G | 1.64985e-05 | 0.0028721 | intron-variant | CHD4 | GRCh38.p7 | 12:6577742 | GACGTTACGCACTTT[C/G]AAGTTTGTCACTTAA | 1108 |
| rs372069898 | snp | C/T | | | intron-variant | CHD4 | GRCh38.p7 | 12:6585347 | TGGAGTGCAGTGGGG[C/T]AATCTTGGCTCACTG | 1108 |
| rs372098743 | snp | A/G | | | intron-variant | CHD4 | GRCh38.p7 | 12:6595940 | TACAGCTTGGTGACA[A/G]AGCAAGACTCCATCT | 1108 |
| rs372129689 | snp | C/T | 0.000197746 | 0.00994152 | intron-variant, nc-transcript-variant | CHD4, SCARNA11 | GRCh38.p7 | 12:6581543 | ACTGAGAGGGAATTG[C/T]TGTGTGTCCTGCCAG | 1108 |
| rs372160129 | snp | A/G | 1.65225e-05 | 0.00287419 | intron-variant | CHD4 | GRCh38.p7 | 12:6578837 | CAATCAACTTCTCCA[A/G]ACACCCACCTTTGTC | 1108 |
| rs372162063 | snp | A/C/G | 6.59482e-05 | 0.00574198 | intron-variant | CHD4 | GRCh38.p7 | 12:6587687 | CCAAGCCCCACACCA[A/C/G]AACGTAAGTTCCTGA | 1108 |
| rs372189643 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | CHD4 | GRCh38.p7 | 12:6594671 | GGATGAAACAGAGAA[A/G]TCAAGAGCTGGCAAG | 1108 |
| rs372219150 | snp | C/G | 1.70452e-05 | 0.0029193 | missense, upstream-variant-2KB | CHD4, SCARNA11 | GRCh38.p7 | 12:6582626 | TCACTTGAACTCTTT[C/G]TCTGATTTGCCTCGC | 1108 |
| rs372281614 | snp | A/C/G | 1.675e-05 | 0.00289391 | intron-variant | CHD4 | GRCh38.p7 | 12:6578163 | ATTTAGGGAAGGTTG[A/C/G]GGGTGGGGGGAAGCA | 1108 |
| rs372282754 | snp | C/G | | | intron-variant | CHD4 | GRCh38.p7 | 12:6595916 | TGAGTCAAGATCACG[C/G]CACTGCACTACAGCT | 1108 |
| rs372315525 | snp | C/T | 1.64768e-05 | 0.00287021 | intron-variant | CHD4 | GRCh38.p7 | 12:6591837 | CTTCCTGAGAACAAA[C/T]GCAAAGAAAAAAGTA | 1108 |
| rs372319960 | snp | A/G | | | intron-variant | CHD4 | GRCh38.p7 | 12:6580128 | AGCTACTCAGAGGCT[A/G]AGGCAGGAGAATCGC | 1108 |
| rs372460785 | snp | G/T | 1.82727e-05 | 0.00302258 | intron-variant, upstream-variant-2KB | CHD4, SCARNA11 | GRCh38.p7 | 12:6582117 | CCCCTAGAAACAATG[G/T]CAAGAGGCTCAGGGC | 1108 |
| rs372480670 | snp | C/G | 1.66233e-05 | 0.00288295 | intron-variant, upstream-variant-2KB | CHD4, SCARNA11 | GRCh38.p7 | 12:6582822 | TATCTGACACTCACC[C/G]CTCCTTAGAATCGTA | 1108 |
| rs372493471 | snp | A/G | 0.000446911 | 0.0149418 | intron-variant, upstream-variant-2KB | CHD4, SCARNA11 | GRCh38.p7 | 12:6582131 | GGCAAGAGGCTCAGG[A/G]CTCACCTTCTTGCGA | 1108 |
| rs372566180 | snp | G/T | | | intron-variant | CHD4 | GRCh38.p7 | 12:6606030 | AGAGCTCCCTCAACT[G/T]GGAACTGCAGAGCAT | 1108 |
| rs372576095 | snp | A/G | 1.66084e-05 | 0.00288165 | intron-variant | CHD4 | GRCh38.p7 | 12:6592573 | TCCAAATTGCTTCAG[A/G]AAGAAAAAGGAAAAA | 1108 |
| rs372617793 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6594245 | ACCCAGGGCTCCATG[A/C/T]CCTCAAATCTTCCGC | 1108 |
| rs372697718 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6593357 | CCAGATCACAAGGAG[A/G]TAAACTAAGCCAGAA | 1108 |
| rs372697811 | snp | A/G | 1.65154e-05 | 0.00287358 | missense | CHD4 | GRCh38.p7 | 12:6598090 | ACATCACCTGACAGT[A/G]CAGCTCCAGCTTTGA | 1108 |
| rs372721338 | snp | C/T | 3.3631e-05 | 0.00410053 | intron-variant | CHD4 | GRCh38.p7 | 12:6600174 | TTACTGTCCCACCCT[C/T]CTTCTCATGGGTTCC | 1108 |
| rs372747762 | snp | C/T | 1.64749e-05 | 0.00287005 | missense | CHD4 | GRCh38.p7 | 12:6599985 | CCGAATTGTCCTCTT[C/T]AGCTTCCCACTGGAT | 1108 |
| rs372752018 | snp | A/T | 0.000153988 | 0.00877328 | synonymous-codon | CHD4 | GRCh38.p7 | 12:6591479 | ACCATTGAAGCGGTC[A/T]ATGGCCTCTTGCCGC | 1108 |
| rs372865017 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CHD4 | GRCh38.p7 | 12:6587055 | TAGATTACCTAGGAT[C/T]TTCTGCCTTTTCTCT | 1108 |
| rs372946963 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | CHD4 | GRCh38.p7 | 12:6597850 | ATCTCTTTAGCAGGA[C/T]TCTCCCACGGAGACT | 1108 |
| rs373036622 | snp | C/T | 1.65378e-05 | 0.00287552 | intron-variant | CHD4 | GRCh38.p7 | 12:6601813 | GCCACCTAGTGCCCA[C/T]ACTTGCTAAGCAAAT | 1108 |
| rs373080026 | snp | C/T | 0.000148386 | 0.00861227 | intron-variant | CHD4 | GRCh38.p7 | 12:6591598 | TCTGCAAAAGAAGCA[C/T]GGTTTAATTATGGAA | 1108 |
| rs373087955 | snp | C/G | | | intron-variant | CHD4 | GRCh38.p7 | 12:6575232 | GCGGGCAGATCACCT[C/G]AGGTCCAGAATTTGA | 1108 |
| rs373098902 | snp | C/T | | | intron-variant, upstream-variant-2KB | CHD4 | GRCh38.p7 | 12:6607242 | GGGTGACGGGATGAC[C/T]CTCGGGGCTGGTAGG | 1108 |
| rs373101952 | snp | C/G | 0.000181388 | 0.00952161 | intron-variant | CHD4 | GRCh38.p7 | 12:6595443 | TCCCTAAAGAAGAAA[C/G]ACATCACACAGCTGC | 1108 |
| rs373195727 | snp | A/G | 0.00175047 | 0.0295325 | intron-variant | CHD4 | GRCh38.p7 | 12:6578971 | AGAACATTCTCCTCT[A/G]TTGCACACTATTATC | 1108 |
| rs373263517 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHD4 | GRCh38.p7 | 12:6586558 | AGCAAGACATCTCTA[A/G]AAACATTTAAAAAAT | 1108 |
| rs373383777 | snp | C/T | | | intron-variant | CHD4 | GRCh38.p7 | 12:6597666 | AGCTTCTCAGGAGGC[C/T]GAGGCAGGATAATCA | 1108 |
| rs373426836 | snp | C/T | | | intron-variant | CHD4 | GRCh38.p7 | 12:6603366 | ACTCCCTCCTCCCTC[C/T]TCTCTCCCTCTTCCC | 1108 |
| rs373427780 | snp | A/C/G | 0.000165172 | 0.00908646 | intron-variant | CHD4 | GRCh38.p7 | 12:6570839 | ATGGTTCTGCAGGAA[A/C/G]AGGTGGTGTCAAGAA | 1108 |
| rs373456261 | snp | G/T | 0.000153988 | 0.00877328 | intron-variant | CHD4 | GRCh38.p7 | 12:6578572 | TGGGGAAGAAAAATG[G/T]CAGCTCCAGCCAAAG | 1108 |
| rs373458230 | snp | A/C | 0.000347939 | 0.0131852 | intron-variant | CHD4 | GRCh38.p7 | 12:6588246 | ATAGAGGCCACTATG[A/C]CTTTCTAGCATAACA | 1108 |
| rs373493199 | snp | A/G | | | intron-variant | CHD4 | GRCh38.p7 | 12:6592367 | AGATGTCTAAATGGA[A/G]TCTGCTTCTGTCCCT | 1108 |
| rs373579535 | in-del | -/GCCCCAGCACACTGCA | | | intron-variant | CHD4 | GRCh38.p7 | 12:6593665 | CCCCAGCACACTGCA[-/GCCCCAGCACACTGCA]ACCCCAGCGAACACC | 1108 |
| rs373584981 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6603396 | CAAGCCACCCCCGCC[C/G]AAAGGGGGGTGGGTA | 1108 |
| rs373587888 | snp | C/T | 1.64947e-05 | 0.00287177 | intron-variant | CHD4 | GRCh38.p7 | 12:6587585 | TCAAGGGCCCACATC[C/T]CCAAAGTCAGTTTCA | 1108 |
| rs373615711 | snp | A/G | 3.29592e-05 | 0.00405938 | intron-variant, downstream-variant-500B | CHD4, SCARNA11 | GRCh38.p7 | 12:6581251 | AGACTGGACTTACAC[A/G]TTTGTCTTTAGTATG | 1108 |
| rs373655516 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | CHD4 | GRCh38.p7 | 12:6609047 | TTCCTGCTCTATACA[A/C]ACCAAGAGTGAAGGC | 1108 |
| rs373676246 | snp | C/T | 4.94956e-05 | 0.00497447 | synonymous-codon, intron-variant | CHD4 | GRCh38.p7 | 12:6600388 | CACAGCAGTCACCTC[C/T]TCCTCGCCTGGGCAA | 1108 |
| rs373705928 | snp | A/C/T | 9.93652e-05 | 0.007048 | intron-variant | CHD4 | GRCh38.p7 | 12:6598195 | CTTCATCGTAGCCCC[A/C/T]ACATCTCCAGACTAT | 1108 |
| rs373736847 | snp | C/T | | | upstream-variant-2KB | CHD4 | GRCh38.p7 | 12:6608074 | ACAACAACGGACACT[C/T]GGCCTCCTCCCACAC | 1108 |
| rs373803693 | snp | A/C | 0.000153988 | 0.00877328 | intron-variant | CHD4 | GRCh38.p7 | 12:6601090 | ATATATACCACAAGA[A/C]CAAAGATGGGGAAAA | 1108 |
| rs373847415 | snp | C/G | 0.000153988 | 0.00877328 | missense | CHD4 | GRCh38.p7 | 12:6602047 | AGGTCCAAGCTTCTT[C/G]TTCTTCTTCTTGCCA | 1108 |
| rs373848458 | in-del | -/A | | | intron-variant | CHD4 | GRCh38.p7 | 12:6599563 | TTCATCTCCTCTTAA[-/A]GAGAGCTGGCAAAAC | 1108 |
| rs373865214 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | CHD4 | GRCh38.p7 | 12:6591654 | AGGTCACTAAGGGTT[A/G]TCTATGACTGTTCCC | 1108 |
| rs373869421 | snp | A/G | 0.000143542 | 0.00847055 | intron-variant | CHD4 | GRCh38.p7 | 12:6573293 | GGGATAAGAGGAAAC[A/G]GGAGTTCGACTGATA | 1108 |
| rs373917645 | snp | C/T | | | intron-variant | CHD4 | GRCh38.p7 | 12:6590778 | GTAGTAAGCCATGAT[C/T]GTGCCACTGCTCTCC | 1108 |
| rs373952266 | snp | C/T | | | intron-variant | CHD4 | GRCh38.p7 | 12:6571292 | CTCTTCTTGAGCTTA[C/T]TCGTTTTTTCTCTTC | 1108 |
| rs374086031 | snp | C/T | 3.58436e-05 | 0.00423326 | intron-variant | CHD4 | GRCh38.p7 | 12:6600876 | ATAGAAGGTCACATC[C/T]TTTCTATTAGACATG | 1108 |
| rs374209480 | snp | C/T | 8.29029e-05 | 0.00643775 | intron-variant | CHD4 | GRCh38.p7 | 12:6596168 | AGAAAACCCTCAGAG[C/T]CAGAAAAGGCAACCC | 1108 |
| rs374271955 | snp | G/T | 3.29462e-05 | 0.00405857 | missense | CHD4 | GRCh38.p7 | 12:6602440 | TTAGGCTTTTTCTTC[G/T]TCTTGAGCTTTGGAG | 1108 |
| rs374348464 | snp | A/G | 4.95536e-05 | 0.00497738 | intron-variant | CHD4 | GRCh38.p7 | 12:6592672 | GCACAATTATGAGCC[A/G]ATTACAGATAAACAC | 1108 |
| rs374378695 | snp | C/T | 1.70177e-05 | 0.00291694 | missense | CHD4 | GRCh38.p7 | 12:6606319 | AAAGTGCATCCATAT[C/T]CTCCTCCTCACTGCC | 1108 |
| rs374451881 | snp | C/T | 1.65537e-05 | 0.0028769 | missense | CHD4 | GRCh38.p7 | 12:6593606 | ACTAGGAAGGGGCCT[C/T]TGGAATGACCCTTTG | 1108 |
| rs374464573 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | CHD4 | GRCh38.p7 | 12:6577979 | CTCAAACTAAAAGAC[C/T]TTCAGAACCTTTCAC | 1108 |
| rs374465950 | snp | G/T | 1.64735e-05 | 0.00286993 | synonymous-codon, upstream-variant-2KB | CHD4, SCARNA11 | GRCh38.p7 | 12:6583267 | CTTTGCCCAGATTTC[G/T]GGCTAGATCTTCTTG | 1108 |
| rs374489035 | snp | A/G | 0.000263552 | 0.0114764 | intron-variant | CHD4 | GRCh38.p7 | 12:6591687 | AAGCTCCCAGTCCAC[A/G]TGATACCTGGGAAAA | 1108 |
| rs374510124 | snp | A/G | | | intron-variant | CHD4 | GRCh38.p7 | 12:6604073 | ATTTGAGGTCAGTTC[A/G]AAACCAGCTTGGCCA | 1108 |
| rs374516089 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | CHD4, SCARNA11 | GRCh38.p7 | 12:6582412 | AGCCCACCACTGCAC[A/G]GGAAGGCTGATCTCT | 1108 |
| rs374584925 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHD4 | GRCh38.p7 | 12:6605554 | CAGCCTAAACCGCAG[A/G]CTACCTCATAGAGAC | 1108 |
| rs374649544 | snp | A/C/G | 1.66829e-05 | 0.00288811 | intron-variant | CHD4 | GRCh38.p7 | 12:6600523 | CACAAATATACAGAA[A/C/G]AGAAACACACCTTTC | 1108 |
| rs374651437 | snp | A/C | | | intron-variant | CHD4 | GRCh38.p7 | 12:6603905 | AAGCTCAGCTTCCTC[A/C]CCACTCCCACCCAGA | 1108 |
| rs374652277 | snp | A/G | 0.000115389 | 0.0075948 | intron-variant, downstream-variant-500B | CHD4, SCARNA11 | GRCh38.p7 | 12:6581444 | TAGATCAGAGAGAAG[A/G]TCATTTCTTCCCAGT | 1108 |
| rs374693470 | snp | C/T | | | intron-variant | CHD4 | GRCh38.p7 | 12:6589275 | GACGAATACTAATAT[C/T]GGTGTGAAAGTTTAA | 1108 |
| rs374889109 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6596725 | GAATTGCTTGAACCC[A/G]GGCGGCGGAGGTTGC | 1108 |
| rs374956325 | snp | C/T | 1.94607e-05 | 0.00311929 | intron-variant | CHD4 | GRCh38.p7 | 12:6573310 | GAGTTCGACTGATAA[C/T]TCACTTTACTCACTT | 1108 |
| rs374977752 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | CHD4 | GRCh38.p7 | 12:6600057 | TTACCCCCACCCGCC[C/T]ACCGCAGTCTGAAGC | 1108 |
| rs375059839 | snp | A/G | 3.45411e-05 | 0.00415564 | intron-variant, upstream-variant-2KB, synonymous-codon | CHD4, SCARNA11 | GRCh38.p7 | 12:6583127 | ATCTGGAGGGAGAGA[A/G]GGCAGATGAGCGGGG | 1108 |
| rs375068038 | snp | A/G | 0.000181427 | 0.00952263 | intron-variant | CHD4 | GRCh38.p7 | 12:6597866 | TCTCCCACGGAGACT[A/G]CCCGTCTCCCGTGTG | 1108 |
| rs375091307 | snp | C/T | 3.40989e-05 | 0.00412895 | missense | CHD4 | GRCh38.p7 | 12:6601024 | CAGGTACACGAGGGC[C/T]GCCCTTGGGCTTCCT | 1108 |
| rs375106320 | snp | A/G | 0.000153988 | 0.00877328 | missense, upstream-variant-2KB | CHD4, SCARNA11 | GRCh38.p7 | 12:6581705 | CCTGGAGTGGAGGGT[A/G]TAGGAGTTTTTGGGG | 1108 |
| rs375234607 | snp | A/G | 0.000153988 | 0.00877328 | missense | CHD4 | GRCh38.p7 | 12:6599774 | GATCAGTCACTCACC[A/G]TACAACGGGGACAGA | 1108 |
| rs375272384 | snp | G/T | | | intron-variant | CHD4 | GRCh38.p7 | 12:6572330 | ACTCGGGAGGCTGAG[G/T]CAGGAGAATTGCTTG | 1108 |
| rs375321825 | snp | C/T | 1.74318e-05 | 0.00295222 | intron-variant | CHD4 | GRCh38.p7 | 12:6594693 | GCTGGCAAGGAACTC[C/T]CCTCCTCCCCTAATA | 1108 |
| rs375331365 | snp | G/T | 6.6291e-05 | 0.00575683 | intron-variant | CHD4 | GRCh38.p7 | 12:6599727 | AGCCTACATAGAAAA[G/T]ACTACACTTTCCCAT | 1108 |
| rs375342857 | snp | C/T | 0.000118814 | 0.00770669 | synonymous-codon | CHD4 | GRCh38.p7 | 12:6594459 | CCCAGATTTCCTTAC[C/T]TCCTTGTAAAGGGAA | 1108 |
| rs375386448 | snp | C/T | 3.29881e-05 | 0.00406115 | utr-variant-3-prime | CHD4 | GRCh38.p7 | 12:6570646 | AGGAAGGTCACTGCT[C/T]AGCGGTGGAGGTGGT | 1108 |
| rs375481328 | snp | A/G | 1.64811e-05 | 0.00287059 | missense | CHD4 | GRCh38.p7 | 12:6601340 | CCTCCACAGGGGGAG[A/G]TGGTGGTGCAACCTC | 1108 |
| rs375485976 | snp | A/C | 4.94287e-05 | 0.00497111 | intron-variant | CHD4 | GRCh38.p7 | 12:6591841 | CTGAGAACAAATGCA[A/C]AGAAAAAAGTATTAA | 1108 |
| rs375492475 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CHD4 | GRCh38.p7 | 12:6572718 | GTGCGTTGCGCCACA[C/T]GCCCAGCTAATTTTT | 1108 |
| rs375639415 | in-del | -/C | | | upstream-variant-2KB | CHD4 | GRCh38.p7 | 12:6607593 | GCCACGCCCCCTTCG[-/C]AGCGGGCGCGCGCGC | 1108 |
| rs375688826 | snp | C/T | 0.000464753 | 0.0152368 | intron-variant | CHD4 | GRCh38.p7 | 12:6578811 | TCTGGTTTTAGAGTT[C/T]TTCTGAACCACAATC | 1108 |
| rs375717948 | in-del | -/A | | | intron-variant | CHD4 | GRCh38.p7 | 12:6591123 | GCAAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 1108 |
| rs375724369 | snp | G/T | 0.000153988 | 0.00877328 | intron-variant | CHD4 | GRCh38.p7 | 12:6588275 | CATGTTACTTATTAA[G/T]GCTGCCTGCTGCCTC | 1108 |
| rs375762397 | snp | C/G | | | intron-variant | CHD4 | GRCh38.p7 | 12:6573330 | TTTACTCACTTCTGA[C/G]TGGCCTCTCAGCTCA | 1108 |
| rs375844456 | snp | C/T | 1.80101e-05 | 0.00300078 | intron-variant | CHD4 | GRCh38.p7 | 12:6598460 | CTTAATCTCAAATCA[C/T]AACCATGGGAGGAGA | 1108 |
| rs375847740 | snp | A/T | 1.64974e-05 | 0.00287201 | intron-variant | CHD4 | GRCh38.p7 | 12:6587594 | CACATCCCCAAAGTC[A/T]GTTTCAGCAGCTGCA | 1108 |
| rs375870008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6587141 | GAGAAAATGACATTC[C/T]GGTAAAGAGCCAAAA | 1108 |
| rs375870161 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CHD4 | GRCh38.p7 | 12:6598960 | GTGCTCAACCTGTAA[C/T]AGAATTCCCTCTCCA | 1108 |
| rs375890776 | snp | A/C | | | upstream-variant-2KB | CHD4 | GRCh38.p7 | 12:6608802 | TTACCTCCAGCTCCT[A/C]AGTTTTGAGGAACAC | 1108 |
| rs375917744 | in-del | -/C | | | intron-variant, downstream-variant-500B | CHD4, SCARNA11 | GRCh38.p7 | 12:6581016 | CTCAAAACAAACAAA[-/C]AAACAAAAAAAATGT | 1108 |
| rs375934665 | snp | A/G | 4.99006e-05 | 0.00499478 | intron-variant | CHD4 | GRCh38.p7 | 12:6592587 | GAAAGAAAAAGGAAA[A/G]AAGTTATTGGAGAAG | 1108 |
| rs375945240 | snp | C/T | 8.51535e-05 | 0.00652453 | synonymous-codon | CHD4 | GRCh38.p7 | 12:6606335 | CTCCTCCTCACTGCC[C/T]GCCGAGCAGGGGGAC | 1108 |
| rs375962772 | snp | A/G | 0.000382171 | 0.0138181 | intron-variant, upstream-variant-2KB | CHD4, SCARNA11 | GRCh38.p7 | 12:6582812 | AAAGATGCAATATCT[A/G]ACACTCACCCCTCCT | 1108 |
| rs376011163 | snp | C/G | 0.000153988 | 0.00877328 | missense, downstream-variant-500B | CHD4, SCARNA11 | GRCh38.p7 | 12:6581305 | CCTCAATGGCAGTCT[C/G]AGGGGCTGTAGATTT | 1108 |
| rs376067533 | snp | A/C/G | 1.72056e-05 | 0.00293301 | intron-variant | CHD4 | GRCh38.p7 | 12:6573279 | TAAGAGCTGGACAAG[A/C/G]GATAAGAGGAAACGG | 1108 |
| rs376127801 | snp | C/T | 0.000115334 | 0.00759299 | intron-variant | CHD4 | GRCh38.p7 | 12:6601619 | CAGAAAGATTCTCCT[C/T]CCCCTTCCCCAAACC | 1108 |
| rs376162433 | snp | A/T | | | upstream-variant-2KB, downstream-variant-500B | NOP2, CHD4 | GRCh38.p7 | 12:6570071 | CCTACACCCACACTG[A/T]ACCAGAGCACTAAAA | 1108 |
| rs376175590 | snp | C/T | 0.000153988 | 0.00877328 | missense, downstream-variant-500B | CHD4, SCARNA11 | GRCh38.p7 | 12:6581140 | CAACAACGACCTTTT[C/T]ATCCTCTGAGGCAGG | 1108 |
| rs376178091 | snp | A/G | 1.64773e-05 | 0.00287026 | synonymous-codon | CHD4 | GRCh38.p7 | 12:6591542 | GTATTTATAACCTTC[A/G]TGTTCCAAGAAATCC | 1108 |
| rs376225091 | in-del | -/C/CAAA | 0.000323313 | 0.0127103 | intron-variant, downstream-variant-500B | CHD4, SCARNA11 | GRCh38.p7 | 12:6581023 | AAACAAACAAACAAA[-/C/CAAA]AAAAATGTGGATACC | 1108 |
| rs376232465 | snp | A/G | | | intron-variant | CHD4 | GRCh38.p7 | 12:6602517 | ATATATTTGGCAAAG[A/G]GTGGTAGGCAGGGAA | 1108 |
| rs376325810 | snp | A/G | 1.66966e-05 | 0.00288929 | intron-variant | CHD4 | GRCh38.p7 | 12:6595481 | CCTTTTCTATAGAAG[A/G]AACAACTTGGCCAGG | 1108 |
| rs376470845 | snp | C/T | 1.64933e-05 | 0.00287165 | missense | CHD4 | GRCh38.p7 | 12:6578861 | CTTTGTCTTCTACCA[C/T]AATAGGGGTCAGATC | 1108 |
| rs376478876 | snp | A/G | 6.65203e-05 | 0.00576678 | intron-variant | CHD4 | GRCh38.p7 | 12:6593249 | CATGAAGGCAACTTG[A/G]TCACTACTAGTCAGT | 1108 |
| rs376601784 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CHD4 | GRCh38.p7 | 12:6583882 | TTATGTCCCAAAAAC[A/G]TTGATACTCCTCTAA | 1108 |
| rs376615408 | snp | C/T | | | intron-variant | CHD4 | GRCh38.p7 | 12:6579827 | TTTGGGAGGCCAAAG[C/T]GGGCGGATCACGAGG | 1108 |
| rs376615761 | snp | A/G | 0.000215045 | 0.0103671 | intron-variant | CHD4 | GRCh38.p7 | 12:6599733 | CATAGAAAAGACTAC[A/G]CTTTCCCATTTTTTG | 1108 |
| rs376623604 | snp | C/T | 1.64754e-05 | 0.00287009 | synonymous-codon, downstream-variant-500B | CHD4, SCARNA11 | GRCh38.p7 | 12:6581054 | TTTACCTTTGGGCTC[C/T]GTCTCCATAGGTTCC | 1108 |
| rs376660921 | in-del | AA/C | | | upstream-variant-2KB | CHD4 | GRCh38.p7 | 12:6608051 | AGAAACTCACCCCCC[AA/C]CCATACTACAACAAC | 1108 |
| rs376667947 | snp | C/T | 8.24042e-05 | 0.00641836 | intron-variant | CHD4 | GRCh38.p7 | 12:6597884 | CGTCTCCCGTGTGCT[C/T]AGCTGGTACCTGTGG | 1108 |
| rs376670062 | snp | A/T | 0.000153988 | 0.00877328 | intron-variant | CHD4 | GRCh38.p7 | 12:6606268 | GGCCCTTGGGGAAGA[A/T]GTTACCTGGGTGGGG | 1108 |
| rs376679386 | snp | A/T | 1.77269e-05 | 0.0029771 | intron-variant, upstream-variant-2KB | CHD4, SCARNA11 | GRCh38.p7 | 12:6582588 | AAGCCCTTGCTCTAG[A/T]TCAGTCCACTCCAGC | 1108 |
| rs376739302 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CHD4 | GRCh38.p7 | 12:6607052 | GGCGAGGGGGTGGGC[A/G]CCGGGCATTGTGGGA | 1108 |
| rs376752804 | snp | A/T | | | intron-variant | CHD4 | GRCh38.p7 | 12:6576028 | GTGAGTTCCGTCCCT[A/T]CTCCAATTCCCTCTC | 1108 |
| rs376775502 | snp | A/G | 1.65853e-05 | 0.00287964 | intron-variant, upstream-variant-2KB | CHD4, SCARNA11 | GRCh38.p7 | 12:6582757 | CAAGTACCTAGGGGA[A/G]GAAGAAACCCAGGTG | 1108 |
| rs376794292 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CHD4 | GRCh38.p7 | 12:6575003 | AGAATTATACAAAAT[C/T]CAAATTGTAATATCC | 1108 |
| rs376798589 | snp | A/G | | | intron-variant, upstream-variant-2KB | CHD4 | GRCh38.p7 | 12:6607266 | TGGTAGGGCCGTGAG[A/G]GGCGTCTCTTTGGGA | 1108 |
| rs376818972 | snp | A/G | | | intron-variant | CHD4 | GRCh38.p7 | 12:6605834 | GATAGAGTGTAACCA[A/G]CACTCCCTCTTTCCT | 1108 |
| rs376819567 | snp | C/T | 9.88566e-05 | 0.00702983 | intron-variant, downstream-variant-500B | CHD4, SCARNA11 | GRCh38.p7 | 12:6581265 | CATTTGTCTTTAGTA[C/T]GGCATTCAGTCACCC | 1108 |
| rs376903288 | snp | C/T | | | intron-variant | CHD4 | GRCh38.p7 | 12:6589126 | GGCAGGCACCTGTAA[C/T]CCCAGCTACTCGGGA | 1108 |
| rs376930091 | in-del | -/A | | | intron-variant | CHD4 | GRCh38.p7 | 12:6595957 | GCAAGACTCCATCTC[-/A]AAAAAAAAAAAAAAG | 1108 |
| rs376945891 | snp | A/G/T | 6.59493e-05 | 0.00574203 | intron-variant | CHD4 | GRCh38.p7 | 12:6591599 | CTGCAAAAGAAGCAC[A/G/T]GTTTAATTATGGAAG | 1108 |
| rs376971060 | snp | C/T | 5.06453e-05 | 0.00503191 | synonymous-codon | CHD4 | GRCh38.p7 | 12:6598402 | GATTAGGATCTTCTG[C/T]ACTTTGCCCTTCAGA | 1108 |
| rs377002874 | snp | C/T | 4.94515e-05 | 0.00497225 | intron-variant | CHD4 | GRCh38.p7 | 12:6577762 | TTGTCACTTAAGCAA[C/T]ATATTCCTCCCCAAC | 1108 |
| rs377091231 | snp | A/G | 0.000661848 | 0.0181793 | intron-variant | CHD4 | GRCh38.p7 | 12:6606223 | AGAGGAGTCACTCGG[A/G]AGAGCCCCAGATGTC | 1108 |
| rs377109723 | snp | C/T | | | intron-variant | CHD4 | GRCh38.p7 | 12:6574169 | AAAAACTGTTTCTGT[C/T]TCCTATGTATGTTTC | 1108 |
| rs377173786 | snp | A/G | 1.64754e-05 | 0.00287009 | missense | CHD4 | GRCh38.p7 | 12:6577840 | AAATTGCCACGGTTC[A/G]TTTCACCCTTGAAAG | 1108 |
| rs377231385 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6604588 | AACCCCCATCAGCTA[C/T]ATCTCACCACCCCCA | 1108 |
| rs377238334 | snp | C/T | 6.58946e-05 | 0.0057396 | missense | CHD4 | GRCh38.p7 | 12:6595404 | AGCTTCTTGCCTGGT[C/T]GGCCTTCCTCACCCC | 1108 |
| rs377286705 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | CHD4 | GRCh38.p7 | 12:6588468 | GTGTCTCCTAAATTC[C/T]AATTCATAAATGTAG | 1108 |
| rs377352005 | snp | G/T | | | intron-variant | CHD4 | GRCh38.p7 | 12:6595069 | GTGCATAAAAGCTAG[G/T]CTATGTGGCCCCTCC | 1108 |
| rs377384385 | snp | C/T | 6.65635e-05 | 0.00576865 | intron-variant | CHD4 | GRCh38.p7 | 12:6595475 | CAAAATCCTTTTCTA[C/T]AGAAGAAACAACTTG | 1108 |
| rs377488166 | snp | C/T | 1.64969e-05 | 0.00287196 | missense | CHD4 | GRCh38.p7 | 12:6600243 | AGCTCCACTTGCCCT[C/T]GGGAGCCTTCTCCAT | 1108 |
| rs377512568 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | CHD4 | GRCh38.p7 | 12:6587346 | GCCAATTTTCAGACC[A/G]ATTACCAAGCACAGG | 1108 |
| rs377545178 | snp | A/G | | | intron-variant | CHD4 | GRCh38.p7 | 12:6579571 | ATCAGCCTGGGCGAC[A/G]GAGCAAGACTCCATC | 1108 |
| rs377625333 | snp | C/T | 1.79187e-05 | 0.00299317 | intron-variant | CHD4 | GRCh38.p7 | 12:6600880 | AAGGTCACATCCTTT[C/T]TATTAGACATGGCAC | 1108 |
| rs377650581 | snp | A/C | | | intron-variant | CHD4 | GRCh38.p7 | 12:6599577 | AAGAGAGCTGGCAAA[A/C]CATCAACTCCTCAGT | 1108 |
| rs377655552 | snp | C/G | | | synonymous-codon | CHD4 | GRCh38.p7 | 12:6606344 | ACTGCCCGCCGAGCA[C/G]GGGGACGGGGAGCCC | 1108 |
| rs377735756 | snp | C/T | 1.6473e-05 | 0.00286988 | missense | CHD4 | GRCh38.p7 | 12:6602389 | ACCTCCTTTTTTTGG[C/T]GCTTGCTCTTAGGGA | 1108 |
| rs377736412 | snp | A/G | 8.23879e-05 | 0.00641772 | synonymous-codon | CHD4 | GRCh38.p7 | 12:6592757 | CCAGATTGTTTTGTA[A/G]TGGTGTCCCAGTCAG | 1108 |
| rs377748407 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CHD4 | GRCh38.p7 | 12:6575308 | CAAAAATTAGTCAGG[A/C]ATGGTGGTACATGCC | 1108 |
| rs386759942 | in-del | A/CAACAACAAC | | | intron-variant | CHD4 | GRCh38.p7 | 12:6580232 | ACTCCATCTCGAAAA[A/CAACAACAAC]AACAACAACAACAAC | 1108 |
| rs386759943 | multinucleotide-polymorphism | AT/CA | | | intron-variant | CHD4 | GRCh38.p7 | 12:6580519 | GGAGACTGGCCTGAC[AT/CA]ATATGGAGAAACCCC | 1108 |
| rs397840945 | in-del | -/C | | | upstream-variant-2KB | CHD4 | GRCh38.p7 | 12:6608053 | AAACTCACCCCCCCC[-/C]ATACTACAACAACGG | 1108 |
| rs397968502 | in-del | -/G | | | intron-variant | CHD4 | GRCh38.p7 | 12:6571733 | GGGAGGCAGAGGCGG[-/G]TGGATCACCTGAGAT | 1108 |
| rs398076393 | in-del | -/A | | | intron-variant | CHD4 | GRCh38.p7 | 12:6590211 | CGAAGAAGAAAAAAA[-/A]ATCTGTATCATATAA | 1108 |
| rs398097969 | in-del | -/A | | | intron-variant | CHD4 | GRCh38.p7 | 12:6577273 | AAAATCCAAAAAAAA[-/A]CAGCTGGGTGTGGTG | 1108 |
| rs527263348 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6571687 | AAAATTAGCTGGGGC[A/G]CAGTGGCTCATGCCT | 1108 |
| rs527303730 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6585365 | TCTTGGCTCACTGCA[A/G]GCTCTGCCTCCCAGG | 1108 |
| rs527340518 | snp | C/G | | | intron-variant | CHD4 | GRCh38.p7 | 12:6600766 | TGGGGACACCAGAAT[C/G]CCAGCAAGCACCGTT | 1108 |
| rs527351783 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6571917 | GGTGAACTGAGATCG[C/T]GCCATTGCTCTCCAG | 1108 |
| rs527375469 | snp | A/G | 0.111576 | 0.20818 | intron-variant | CHD4 | GRCh38.p7 | 12:6579078 | CCAGCATCTTGGGAG[A/G]CAGCAGCAGGCAGAT | 1108 |
| rs527412973 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6572257 | ATGGTGAAACTCCAT[C/G]TCTACTAAAAATACA | 1108 |
| rs527455442 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | CHD4 | GRCh38.p7 | 12:6603892 | CAAGAAGTCTCTGAA[C/G]CTCAGCTTCCTCACC | 1108 |
| rs527467235 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6597133 | AAAAAAAAATTAGCC[A/C]GGCATGGTGGCGATG | 1108 |
| rs527489005 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6597518 | CTGTTAATCCTAGCA[A/C]TTAGGGAGGCCAAGG | 1108 |
| rs527501940 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CHD4 | GRCh38.p7 | 12:6590849 | AACAAAACAGGCTGG[A/G]CGTGGTGGCTCGTGC | 1108 |
| rs527656253 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHD4 | GRCh38.p7 | 12:6598627 | CATCCTAGCTAACAT[A/G]GTGAAACCCCGTCTC | 1108 |