| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs534465877 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36381279 | GTGCATGCCACCATG[C/T]CTGGCTGATTTTTTT | 8208 |
| rs534495134 | snp | A/G | | | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36378485 | TGGATCATGAGGTCA[A/G]GAGATCGAGACCATC | 8208 |
| rs534555310 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CHAF1B | GRCh38.p7 | 21:36407431 | TGCAGTAAATATTAT[A/G]CAGCTACAAAAAAAT | 8208 |
| rs534617963 | snp | A/C | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36398141 | CACTGCAGCTTTGAC[A/C]TCCTGGGCTCGAGCA | 8208 |
| rs534650158 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36380135 | GCCATCTGCCCGCCT[C/T]GGCCTCCCAAAATGC | 8208 |
| rs534735430 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36406955 | AGGTAAAAATAGAAA[A/G]CTCTTGTAAGGAAAT | 8208 |
| rs534739534 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CHAF1B | GRCh38.p7 | 21:36400421 | GGTTGCAGTGAGCTG[A/T]AATCACACCATTGCA | 8208 |
| rs534777206 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36408467 | TGCCTGGAGGCTCAA[C/T]GGTGCCCTATGGCAA | 8208 |
| rs534798407 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36408223 | GTGTAGAAGAGCTCT[C/T]AGATGGGGACTGTTC | 8208 |
| rs534862455 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36414338 | TCTCAGCCTCTCCTG[C/T]GCCAATAGGTCTTCT | 8208 |
| rs534893618 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36413718 | ACACCTCTTCCTCTT[G/T]GTGATGCCAGGAGTC | 8208 |
| rs534986698 | snp | C/T | | | upstream-variant-2KB, intron-variant | CHAF1B | GRCh38.p7 | 21:36383805 | AGGCGCCCGCCGCCA[C/T]GCCCGACTAATTTTT | 8208 |
| rs535072634 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36393940 | AGTCTCACTCTGTTG[C/T]GCAGGCTGGAGTGCA | 8208 |
| rs535073093 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36381258 | CCAAGTACCTGGGAC[-/T]TATAGGTGCATGCCA | 8208 |
| rs535081890 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | MORC3 | GRCh38.p7 | 21:36376881 | AGCACTTTGGGAGGC[C/T]GAGGCGGGCGGATCA | 8208 |
| rs535086385 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36387308 | GCTCAGTGCAGCCCC[A/G]ACCCGGGGCTCAAGT | 8208 |
| rs535229409 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CHAF1B | GRCh38.p7 | 21:36392786 | GCGGCCGGGCAGAGA[C/T]GCTACTCACTTCCTA | 8208 |
| rs535316100 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CHAF1B | GRCh38.p7 | 21:36396318 | ATTTTAGGTTTTATC[A/G]TAAGTGTGATGGGTT | 8208 |
| rs535400545 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36402634 | ACTATGTAAAGAAAA[C/T]CATAGGCACATATAG | 8208 |
| rs535409567 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-3-prime | CHAF1B | GRCh38.p7 | 21:36416670 | TCCTCCCTGGCATCC[C/T]CGTGAAAGTGCACAC | 8208 |
| rs535412302 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36410550 | CCCTTTCTTCTGCAT[G/T]CTCTGCCCTTGGTCC | 8208 |
| rs535496439 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHAF1B | GRCh38.p7 | 21:36409867 | TCAGTTTTTTTTTTT[C/T]TTTCTTTCTTCAGGA | 8208 |
| rs535556206 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36391151 | AGTGGCATTTGCTGG[C/T]CTAGGGACCCTTCTG | 8208 |
| rs535634822 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B | MORC3 | GRCh38.p7 | 21:36376833 | TCAAAAGCTTTTTCT[C/G]AGCCTGGCGCAGTGG | 8208 |
| rs535650241 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36381818 | GTCCCATGATCTGCT[C/G]TCTGCAAGATGGAGA | 8208 |
| rs535746777 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36389056 | AGTGCCGGTCGGGGT[A/G]AGATCCCGCGTCGGT | 8208 |
| rs535791702 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36401998 | CGCCCGCCTTGGCCT[A/C]CCAAAGTGCTGGGAT | 8208 |
| rs535797140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36407349 | GCTTATTGCAAGCAT[C/T]GTTTATAGTGGTAAA | 8208 |
| rs535881261 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36413588 | TCCAGGACTGTGGCC[A/G]CTCTCTCTCCTGAGT | 8208 |
| rs535887188 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36406488 | ATGAGGTTTTACCAT[G/T]TTGGCCAGGGTGGTC | 8208 |
| rs535924263 | snp | A/G | 1.66676e-05 | 0.00288679 | missense | CHAF1B | GRCh38.p7 | 21:36413134 | ACTCCCCCTCAGGCC[A/G]GACAGGCCCCAGCCC | 8208 |
| rs536060765 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36398213 | GTGCACCACCACACC[C/T]GGCTAATTTTTATAT | 8208 |
| rs536097704 | in-del | -/TA | 0.000644783 | 0.0179437 | intron-variant | CHAF1B | GRCh38.p7 | 21:36387564 | AATATGTGCCCATTC[-/TA]TGTTTTTCAAATGAA | 8208 |
| rs536115732 | snp | A/G | 1.65671e-05 | 0.00287807 | intron-variant | CHAF1B | GRCh38.p7 | 21:36386270 | ATGTCAGGGTAAACT[A/G]GGGCAGAGATAGACA | 8208 |
| rs536124420 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36396093 | GCAACCTCTGCCTCC[C/T]GGGTTCAACAATTCT | 8208 |
| rs536132733 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36407737 | AATCCCAGCACTTTG[A/G]GAGGCGGAGGAGGGC | 8208 |
| rs536152511 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | CHAF1B | GRCh38.p7 | 21:36385066 | GGTTGTGTTAGCCCT[C/T]CAAGTGCCCAGCGCC | 8208 |
| rs536273178 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHAF1B | GRCh38.p7 | 21:36391969 | TCTTGGGTGTTTCTC[A/G]GAGAGGGGGATTTGG | 8208 |
| rs536333514 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36389803 | TGTGTGTGTGTGTGC[A/G]CGCGCACGCTGATTT | 8208 |
| rs536363321 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHAF1B | GRCh38.p7 | 21:36397688 | AATTAATTAGGACAA[A/G]TGCCTTACACGAAGT | 8208 |
| rs536409942 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36414849 | AACTCCTGACCTCAA[A/G]TGATCTGCCCGCCTC | 8208 |
| rs536537249 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36381873 | TAGTCCCACTCCAAA[G/T]CCCTGAGAACCAGGG | 8208 |
| rs536599381 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | CHAF1B | GRCh38.p7 | 21:36383583 | ATGGATGCTTGGGGC[C/T]CAAGCTGAACAACAG | 8208 |
| rs536676547 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHAF1B | GRCh38.p7 | 21:36395320 | CCCAAAGTGCTGGGA[C/T]TACAGGCATGAGCCA | 8208 |
| rs536742024 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CHAF1B | GRCh38.p7 | 21:36401983 | TGGACTCAAGTGATC[C/T]GCCCGCCTTGGCCTC | 8208 |
| rs536921780 | snp | C/G | 1.64944e-05 | 0.00287175 | intron-variant | CHAF1B | GRCh38.p7 | 21:36411452 | ACTTTGTCTCTGTCC[C/G]CAACCCCCAGGTGTG | 8208 |
| rs536944753 | in-del | -/GGG | 0.00358779 | 0.0422022 | intron-variant | CHAF1B | GRCh38.p7 | 21:36396328 | TATCATAAGTGTGAT[-/GGG]GGGTTGTTACTGAAC | 8208 |
| rs536955958 | snp | G/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36411790 | CTGGAGTGCAGTGGT[G/T]TGATCTCGTTTCACT | 8208 |
| rs536990920 | snp | A/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 21:36377339 | AAAATTAATCATGGG[A/T]TTAGTAAGAGAAACT | 8208 |
| rs537009952 | snp | A/G | | | downstream-variant-500B | MORC3 | GRCh38.p7 | 21:36376694 | TTTAAAACTAAAAAT[A/G]TATTCATTAGACCCT | 8208 |
| rs537073216 | snp | C/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36406478 | TTTAGTAGAGATGAG[C/G]TTTTACCATGTTGGC | 8208 |
| rs537084207 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36389168 | TGGTGTCTGCAGTGC[C/T]GGGCTGCTGGAGGGT | 8208 |
| rs537402126 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36411889 | GCGCACCACTACGCC[C/T]GGCTAATTCTTGTGG | 8208 |
| rs537419667 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36414398 | GCTGGCTTTAACGCC[C/G/T]TCTTAAAATCTCTCA | 8208 |
| rs537451637 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CHAF1B | GRCh38.p7 | 21:36392152 | ATGCTGCCTTCAAGC[A/G]TCTGTTTAACAAAGC | 8208 |
| rs537552190 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36388118 | GTGAGCCACTGCGCC[C/T]GGCCTGGATATGCTT | 8208 |
| rs537679755 | snp | C/T | 0.0588605 | 0.161139 | intron-variant | CHAF1B | GRCh38.p7 | 21:36393267 | AGGATTTTTAAATTT[C/T]TGTGGAGACAGGGTC | 8208 |
| rs537762285 | snp | C/T | 1.64746e-05 | 0.00287002 | synonymous-codon | CHAF1B | GRCh38.p7 | 21:36399539 | GCTGCGAGTATACAG[C/T]ATACAGAAGAAGCGT | 8208 |
| rs537912573 | snp | A/C | 0.000165631 | 0.00909881 | | | GRCh38.p7 | 21:36377424 | GATATTGAAGTATTG[A/C]CAAGATATGAGACTT | 8208 |
| rs537927899 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CHAF1B | GRCh38.p7 | 21:36410672 | TTTCCTCTTGCTGCT[G/T]TCTTTTTTTTTTTTT | 8208 |
| rs537945656 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | MORC3 | GRCh38.p7 | 21:36376998 | TGCATGCCTGTAATC[C/T]CAGCTACTCAGGAGG | 8208 |
| rs537954202 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | CHAF1B | GRCh38.p7 | 21:36383837 | GTAATTTTTGTAGAG[A/G]TGGGGTTTCACCATG | 8208 |
| rs538066205 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36378539 | TCTCTACTAAAAATA[C/T]AAAAATTAGCTGGGC | 8208 |
| rs538121934 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CHAF1B | GRCh38.p7 | 21:36382542 | TCTTTTTCTTTCTTT[C/T]TTTTTTTTTTTTTTT | 8208 |
| rs538134939 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36388102 | TGTTGGGATTACAGG[C/T]GTGAGCCACTGCGCC | 8208 |
| rs538156719 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36381874 | AGTCCCACTCCAAAG[C/T]CCTGAGAACCAGGGA | 8208 |
| rs538194358 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36396437 | CCAGCACTTTGGGAG[C/G]ATTGCTCAAGCCTAG | 8208 |
| rs538242657 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CHAF1B | GRCh38.p7 | 21:36400364 | TGATCCCAGCTATTC[A/G]GGAGGCTGAGGCAGG | 8208 |
| rs538242740 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36393327 | AGAAGTTTTATTTAT[A/G]TGAAACAGTCCTAAG | 8208 |
| rs538278399 | in-del | -/AACAAGTGAACAAGGGTCTCTGGTTTTCCTAGGCAGAGG | 0.00716551 | 0.0594257 | intron-variant | CHAF1B | GRCh38.p7 | 21:36392024 | GAAGGTCAGCAGATA[lengthTooLong]AACAAGTGAACAAGG | 8208 |
| rs538280508 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36411360 | CTCAAGTGATCCACC[C/T]GGCTCGGCCTCCCAA | 8208 |
| rs538290324 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36408432 | AGCTGAATCTAGTCA[C/T]GGTGCTTCAATCGAG | 8208 |
| rs538478053 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36415636 | GCTCAGGTTTCTCCA[C/T]CTGATGACTGCTGAC | 8208 |
| rs538525084 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36392457 | ACCTCCCAGACGGGG[C/T]GGCGGCCGGGTAGAG | 8208 |
| rs538553568 | snp | A/G | 0.0023933 | 0.0345097 | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36378851 | CAGGAATTTATACTT[A/G]GGATGAGTAATAAAT | 8208 |
| rs538726344 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CHAF1B | GRCh38.p7 | 21:36385246 | CGGGATTCCGACCCC[A/G]GGGCCAGAGCAGGAC | 8208 |
| rs538742086 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CHAF1B | GRCh38.p7 | 21:36410809 | AGGATTACAGGTGTG[C/T]GCCACCACACCCAGC | 8208 |
| rs538744955 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | CHAF1B | GRCh38.p7 | 21:36407375 | GTAAAAAACCAAAAG[C/G]CAAAAAAATACTCAT | 8208 |
| rs538763908 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CHAF1B | GRCh38.p7 | 21:36392476 | GGCCGGGTAGAGGGG[A/C]TCCTCACTTCCCAGA | 8208 |
| rs538791707 | snp | A/G | | | intron-variant, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36381475 | CTAAAAGAGACTATA[A/G]TATAGTCTCTTTTGC | 8208 |
| rs538853973 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | CHAF1B | GRCh38.p7 | 21:36383391 | GTGAGCCACCATGCC[C/T]GGCTCAGATTTTGAT | 8208 |
| rs538945996 | in-del | -/A | 0.338296 | 0.233889 | intron-variant | CHAF1B | GRCh38.p7 | 21:36407301 | AGTGAGACTCTGTCT[-/A]AAAAAAAAAAAAAAA | 8208 |
| rs538958970 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CHAF1B | GRCh38.p7 | 21:36392542 | GACGGGGCAGCTGGC[C/T]GGGCGGGGGCTGCCC | 8208 |
| rs539042922 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHAF1B | GRCh38.p7 | 21:36382611 | GTGGCATGATCTTGG[C/T]TCACTGCCCTCTGGG | 8208 |
| rs539128820 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36390377 | CAAAGAATGGGAATG[C/T]GTATGTCCTCACAAC | 8208 |
| rs539152209 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36399086 | CTGTTGCCCAGGCTG[A/G]AGTGCAGTGCCACAA | 8208 |
| rs539193645 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36396198 | AGAGATGGGGTTTGC[C/G]CATGTTGGCCAGGCT | 8208 |
| rs539229865 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | CHAF1B | GRCh38.p7 | 21:36398365 | TATTTTTATTTTTTT[A/T]AAATTGTTTTTTGAG | 8208 |
| rs539243544 | snp | A/G | | | missense, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36386174 | TAGCCTGGCACAACA[A/G]GGAGCCCGTGTACAG | 8208 |
| rs539407186 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36415530 | CCATTGTTTAAACCC[A/G]CCGGCTGCCTGTTTA | 8208 |
| rs539524379 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHAF1B | GRCh38.p7 | 21:36389981 | CATCCATCAGGGCCA[A/G]TGGCATGTTAACCAA | 8208 |
| rs539549217 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36413747 | TCTCCTGAAAGACCC[A/G]TTTCAATGTACCCTC | 8208 |
| rs539626282 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36388813 | AAAGAATTCAGCAAT[A/G]GCAAAGTTCCTCATG | 8208 |
| rs539641445 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHAF1B | GRCh38.p7 | 21:36395455 | CTATGGATTGTCAGA[A/G]GGTAAGAGGCTTAGC | 8208 |
| rs539656452 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | CHAF1B | GRCh38.p7 | 21:36382544 | TTTTTCTTTCTTTTT[C/T]TTTTTTTTTTTTTCA | 8208 |
| rs539678746 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36401987 | CTCAAGTGATCCGCC[C/T]GCCTTGGCCTCCCAA | 8208 |
| rs539764252 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CHAF1B | GRCh38.p7 | 21:36400968 | AGGTCACACCTGTGA[A/T]GTAAGAATAGTAATG | 8208 |
| rs539871948 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | CHAF1B | GRCh38.p7 | 21:36414975 | TATATATAGAAACCA[C/T]ATCTGACTGCCTTTT | 8208 |
| rs539927612 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36403757 | GATAAGGCTAGGCAT[G/T]ATTGTGGCCACAGTG | 8208 |
| rs540026619 | in-del | -/TTG | 0.00119737 | 0.0244387 | intron-variant | CHAF1B | GRCh38.p7 | 21:36398730 | TTCTGAAAAGAAGTC[-/TTG]TTGTCGTGTTTACTG | 8208 |
| rs540041198 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | CHAF1B | GRCh38.p7 | 21:36417017 | ATTTTATTTCATATG[C/T]AATTTGGTATCTAAA | 8208 |
| rs540159491 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | MORC3 | GRCh38.p7 | 21:36376418 | ACATTCAATCCGTTC[A/G]TTTTGTATGTATGCT | 8208 |
| rs540199138 | snp | A/C | 0.0023933 | 0.0345097 | downstream-variant-500B | MORC3 | GRCh38.p7 | 21:36377133 | AAAAAAAGGACTTTT[A/C]TTTGTATAAATCATT | 8208 |
| rs540254724 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36383085 | TATGTCTGTTATCAA[A/G]GCTTTTTTTTTTTTT | 8208 |
| rs540266062 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36390748 | GCAGCCTCCACCTCC[C/T]GGGCTCAAGTGATCC | 8208 |
| rs540270296 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36397335 | AAGGGAATAATATTT[A/G]AGTCATAGTTTATAC | 8208 |
| rs540271113 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHAF1B | GRCh38.p7 | 21:36404464 | TTTGAGATGGAGTTT[C/T]GCTCTTGTTACCCAG | 8208 |
| rs540307948 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36411959 | GTATCAAACTCCTGG[G/T]CTCAACGATCCTCCT | 8208 |
| rs540338213 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36409089 | CAAACTGCTGACCTC[A/G]AGTGGTCCGCTTGCC | 8208 |
| rs540349832 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36396487 | GCAACATGGCAAAAC[C/T]CTCTCTCTACCAAAA | 8208 |
| rs540433867 | in-del | -/AC | 0.0162398 | 0.0886349 | downstream-variant-500B | CHAF1B | GRCh38.p7 | 21:36417295 | CATATATATATATAT[-/AC]ACACACACACACAAG | 8208 |
| rs540485646 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B | MORC3 | GRCh38.p7 | 21:36377103 | CTGGGCAACAAGAGC[A/G]AAACTCCGTCTCAAA | 8208 |
| rs540520741 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36402201 | GCATGTGCCTGTAGT[C/G]CCAGGAGGCTGAGAC | 8208 |
| rs540524397 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CHAF1B | GRCh38.p7 | 21:36383633 | TTAGAATTGCGTTAT[A/G]GGAATTCCCTTTTTT | 8208 |
| rs540555646 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CHAF1B | GRCh38.p7 | 21:36410021 | CAGGCTGGAGTGCAG[G/T]GGTGCAATCTTGGCT | 8208 |
| rs540662217 | snp | C/G/T | 6.59059e-05 | 0.00574014 | intron-variant | CHAF1B | GRCh38.p7 | 21:36387757 | TGTCCTTCAGAGATT[C/G/T]TTCGGGAACCAGATA | 8208 |
| rs540837944 | snp | C/T | | | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36378267 | TGCGTATATTTGTGT[C/T]GATATTTACACAGTG | 8208 |
| rs541029865 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CHAF1B | GRCh38.p7 | 21:36405984 | AGTGATACTTGGGAG[C/G]GCATTTGCCTCACCA | 8208 |
| rs541238064 | in-del | -/TAAA | 0.00159617 | 0.0282053 | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36378805 | TATGCCATGTACATT[-/TAAA]TAAATATTGCCATCC | 8208 |
| rs541276719 | in-del | -/TCTCAGCTACC | 0.00199481 | 0.0315187 | intron-variant | CHAF1B | GRCh38.p7 | 21:36396992 | GTACCCATTAGCAGT[-/TCTCAGCTACC]TCTCCCTGCTCCATA | 8208 |
| rs541290414 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36384398 | GAATCATGGGGCTGA[A/G]TAGGGCCAGGAATCT | 8208 |
| rs541310614 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36396829 | TCGGTCACCTCCTAA[C/G]TAGTGACCCTCTTTG | 8208 |
| rs541438540 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36412694 | CTAGTAGCACAGATA[A/G]GTTGCAGCGACTTAG | 8208 |
| rs541601358 | snp | C/G | 0.00358779 | 0.0422022 | utr-variant-5-prime, intron-variant | CHAF1B | GRCh38.p7 | 21:36385409 | GAAGCGGCGCGCGCT[C/G]CGCGGGAGGTGACGG | 8208 |
| rs541689046 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CHAF1B | GRCh38.p7 | 21:36415792 | CAGTCTTGCTCTGTC[A/G]CCCAGGCTGGAATGC | 8208 |
| rs541762672 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36388042 | TGGTCAGGCTGATCT[C/T]GAACTCCTGACCTCA | 8208 |
| rs541815120 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36410858 | TAGAGGCAGGGTTTT[G/T]CCATGTTGGCCAGTC | 8208 |
| rs541851843 | snp | A/C | 0 | 0 | intron-variant | CHAF1B | GRCh38.p7 | 21:36410155 | TTTAGTAGAGATGGG[A/C]TTTTGCCATGTTGGC | 8208 |
| rs541896166 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CHAF1B | GRCh38.p7 | 21:36409151 | TGAGTCATTGCACCC[A/G]GCTTGTATTTTTTTT | 8208 |
| rs541934026 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36415840 | TCACTGCAGCCTCCA[C/T]CTCCCACGTTCAAGC | 8208 |
| rs542046128 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36382173 | ATGTCTTAGCCCGGG[A/C]AAACTGAGGCATAAA | 8208 |
| rs542082814 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36390023 | AATGTGTGCGAATAG[A/G]ATTCCGGTTAACTTA | 8208 |
| rs542121327 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | CHAF1B | GRCh38.p7 | 21:36395855 | AATTCTACAACTCAA[G/T]TACCTGGGTAGGGCA | 8208 |
| rs542195883 | snp | A/C | | | upstream-variant-2KB, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36384457 | AGTATATAGTCATTC[A/C]CAGTCCAAGCTCTGT | 8208 |
| rs542295632 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36405762 | AGAAAGGGGCAGGAC[A/C]TTTATGGAGAAGTCT | 8208 |
| rs542337327 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36398006 | TGGGATTACAGGCAT[A/G]AGCCACCATGCCCCG | 8208 |
| rs542381658 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHAF1B | GRCh38.p7 | 21:36404558 | TCCTGCCTCAGCCTC[C/T]GGAGTAGCTGGGATT | 8208 |
| rs542418147 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36412019 | AGGCGTGAGCCACCA[C/T]GCCCGGCCCCAATTT | 8208 |
| rs542506026 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36411713 | ATGGCTTTGGGGGAC[A/G]TATTCACCAATTTTG | 8208 |
| rs542583132 | snp | C/T | 0 | 0 | downstream-variant-500B | CHAF1B | GRCh38.p7 | 21:36417084 | AAAGTATCTTTTTTG[C/T]TTTTTGAGACAGGGT | 8208 |
| rs542635972 | snp | G/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36406407 | TCTTCTGCCTCAGCC[G/T]CCCAAGTAGCTGGGA | 8208 |
| rs542647499 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | CHAF1B | GRCh38.p7 | 21:36383704 | CCCAGGCTGGAGTGC[A/G]GTGGCACGATCTCGG | 8208 |
| rs542917898 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 21:36377559 | GACAGTATTGCTTCA[A/G]CTAATGTTTATTACT | 8208 |
| rs542931023 | snp | A/G | 0.000791087 | 0.0198725 | intron-variant | CHAF1B | GRCh38.p7 | 21:36402892 | AGGAATGATGGCCGA[A/G]TGGGGATGTCTGCTC | 8208 |
| rs543011421 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36381163 | TCTTGCTCTGTTGCC[C/T]AGGCTGGAGTACAAT | 8208 |
| rs543048299 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36380621 | GCTCTTGCTTTGTCA[A/C]CCAGGCTCGAGTAGC | 8208 |
| rs543171010 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36387904 | ACTCACTGCAACCTC[C/T]GCCTCCTGGGTTCAA | 8208 |
| rs543208626 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CHAF1B | GRCh38.p7 | 21:36394211 | CCTCCTGAGTAGCTG[A/G]GTCTGCAGGTGTGCA | 8208 |
| rs543244183 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | CHAF1B | GRCh38.p7 | 21:36403476 | AAAAAAAAAAAAAAA[A/G]AAAAGAAACTTTACT | 8208 |
| rs543644656 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36393733 | TGCTGGGATTACAGG[C/T]GTGAGCCACTGCGAC | 8208 |
| rs543683331 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36399894 | ATTACAAATATGGGT[A/G]CTGGCCGGGCGCCGT | 8208 |
| rs543684768 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | CHAF1B | GRCh38.p7 | 21:36400466 | ACAAGAGCGAAACTC[A/C]GTCTCAAAATAAATA | 8208 |
| rs543775894 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | CHAF1B | GRCh38.p7 | 21:36392861 | GAGGCCAAGGCAGGC[A/G]GCTGGGAGGTGGAGG | 8208 |
| rs543805385 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36407743 | AGCACTTTGGGAGGC[A/G]GAGGAGGGCAGATCA | 8208 |
| rs543813111 | snp | A/G | | | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36380123 | TTCTGGCCTAAAGCC[A/G]TCTGCCCGCCTCGGC | 8208 |
| rs543841666 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36407147 | TCTCTACTAAAAATA[C/G]AAAAATTAGCCGGGC | 8208 |
| rs543955673 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CHAF1B | GRCh38.p7 | 21:36411099 | ATGCTGGATGTATTT[C/T]TATTCTTATAAATAT | 8208 |
| rs544064482 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36386656 | CTACTTTGTCATCTA[G/T]CCCAGAATGCTAAAT | 8208 |
| rs544149538 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36385484 | CGGGCAGCTCCGCGG[C/T]TCTTTTGGTCGCGTC | 8208 |
| rs544186573 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36403549 | TGTATGGAAGCCATA[A/G]CGCTAAAGCCAAAGA | 8208 |
| rs544200530 | snp | G/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36393266 | GAGGATTTTTAAATT[G/T]CTGTGGAGACAGGGT | 8208 |
| rs544236029 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36390041 | TCCGGTTAACTTAGC[A/G]TGGGAATGCAGGCTG | 8208 |
| rs544281789 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | CHAF1B | GRCh38.p7 | 21:36416858 | TGATTTTAAAGGTGA[C/T]GATGCTTATTCTTTT | 8208 |
| rs544337389 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CHAF1B | GRCh38.p7 | 21:36389191 | TGGAGGGTGCTGGGG[A/G]GGGAGCATACCGGGA | 8208 |
| rs544358552 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36409930 | ATGGACGTACTCCTT[C/T]TGTTTGTCTATGTCT | 8208 |
| rs544416680 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | MORC3 | GRCh38.p7 | 21:36376126 | ATGTGAGTTGAGGAA[A/G]ACAGTCTTTCTCAAA | 8208 |
| rs544448994 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36409237 | AACTCCTGACCTCAG[G/T]TGATCCGCCTGCCTC | 8208 |
| rs544452367 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CHAF1B | GRCh38.p7 | 21:36382862 | CAGGTGCCTGCCACC[A/G]CGCCTGACCTATTTT | 8208 |
| rs544530373 | in-del | -/AAAT | 0.00358779 | 0.0422022 | intron-variant | CHAF1B | GRCh38.p7 | 21:36400472 | CGAAACTCAGTCTCA[-/AAAT]AAATAAATAAATAAA | 8208 |
| rs544538268 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CHAF1B | GRCh38.p7 | 21:36382240 | AGAATACCGTGGTAT[C/G]AATATGGCACAGTCT | 8208 |
| rs544711694 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CHAF1B | GRCh38.p7 | 21:36394982 | GTGATCTGCCCGCCT[C/T]AGCCTCCCAAAGTGC | 8208 |
| rs544762979 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36398679 | TATTTTAATGACTCC[A/G]TTTAAATGGATATAA | 8208 |
| rs544832837 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36406598 | GCCTCCTTTTTTTTT[G/T]AATTGACAGATGAAA | 8208 |
| rs544981478 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36386780 | GTGCAGTGGTGCAAT[C/G]TCGACTTACTGCAAC | 8208 |
| rs544996440 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36378398 | CTTACTTACTTTTCG[G/T]TAGAAAGAATATACT | 8208 |
| rs545067377 | snp | A/G | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 21:36377719 | TTCCTTTGGGCCTCA[A/G]ATTCTTCATGTGGCA | 8208 |
| rs545076336 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CHAF1B | GRCh38.p7 | 21:36384108 | TGAAGTCGGATCTCT[A/G]AAATGTTCGCCAAGA | 8208 |
| rs545170876 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36408490 | TATGGCAAAGGCTCA[C/T]TATGTTCTCCTCGCC | 8208 |
| rs545264229 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CHAF1B | GRCh38.p7 | 21:36383750 | GCTTCCCGGGTTCAC[A/G]CCATTGTCTTGCCTC | 8208 |
| rs545270565 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36412632 | CTCCCAAAGTGCTGG[C/G]ATTACAGGCGTGAGC | 8208 |
| rs545302232 | in-del | -/AGAA | 0.00279162 | 0.0372561 | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36378400 | TACTTACTTTTCGTT[-/AGAA]AGAATATACTGGCTG | 8208 |
| rs545307914 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36406108 | CCAGAAAAAGATCTC[A/G]GGATATAAGGCGATT | 8208 |
| rs545489605 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36384281 | TTTATGTTTGAGAGA[C/T]ACGAAGAATCCAGAG | 8208 |
| rs545577454 | snp | A/G | 0.000801282 | 0.02 | intron-variant | CHAF1B | GRCh38.p7 | 21:36392024 | GGAAGGTCAGCAGAT[A/G]AACAAGTGAACAAGG | 8208 |
| rs545584153 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36381257 | TCCCAAGTACCTGGG[A/C]CTATAGGTGCATGCC | 8208 |
| rs545650278 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHAF1B | GRCh38.p7 | 21:36397822 | AACCTCTGCCTCCTG[A/G]TTTCAAGCGATTCTC | 8208 |
| rs545735961 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36397249 | ATGAAGTCATCTTTG[C/T]GACCCCAGAGCCTGA | 8208 |
| rs545787175 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36415707 | GTGTATTATGCGATG[A/T]TTAACAGCATCCCCG | 8208 |
| rs545937455 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36403102 | AGATTTCCAAGTGAT[C/T]GTAATGTGCAGAAAA | 8208 |
| rs545968159 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36414458 | ACAATTTTTCTGTTT[C/G]TTTTTATGTGACGGA | 8208 |
| rs545969022 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36380674 | ACAGCCGCAATCTCC[C/T]GGGCTCAGGTAATCC | 8208 |
| rs546006231 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36388620 | TACAGGCGCCTGCCA[C/T]CACCCCCGGCTAATT | 8208 |
| rs546054456 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36394774 | TCTCACTCTGCCGCC[C/T]AGGCTGGAGTGCAGT | 8208 |
| rs546141329 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36394296 | TGGCCAGGATGGTCT[C/T]GATCTCCCGACCTTG | 8208 |
| rs546180171 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHAF1B | GRCh38.p7 | 21:36400530 | GATGCCTTGGCCCCA[A/G]CCTGAGTGGCGTGAT | 8208 |
| rs546241885 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CHAF1B | GRCh38.p7 | 21:36383310 | CATGTTGGCCAGGCT[G/T]GTCTGGAACTCCTAG | 8208 |
| rs546267917 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CHAF1B | GRCh38.p7 | 21:36399972 | TCACTTGAGGTCAGG[A/G]GTTTGAGACCAGCCT | 8208 |
| rs546352733 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36413977 | CTCCAGCAGCCTGGT[C/T]GGTGAGAAACGGAGG | 8208 |
| rs546567321 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CHAF1B | GRCh38.p7 | 21:36410482 | TTTTTGTTTTTTTCT[C/T]CTTCCAGTGTTTGAT | 8208 |
| rs546602863 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CHAF1B | GRCh38.p7 | 21:36415538 | TAAACCCGCCGGCTG[C/T]CTGTTTACGCCTCAG | 8208 |
| rs546656541 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36391109 | AGGTTATGCCTTCAG[A/G]TTTATTAATGTAGCC | 8208 |
| rs546665634 | snp | C/T | | | intron-variant, upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36381333 | TTGCTACGTTGCCCA[C/T]GCTGGTCTTGAACTC | 8208 |
| rs546712986 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36410388 | CTGTTATTCCCTTCT[C/T]TTATTCAAATACTCC | 8208 |
| rs546775148 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36411208 | AACCTCCGCCTCCTG[G/T]GTTCAAGCGATTCTC | 8208 |
| rs546780647 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | CHAF1B | GRCh38.p7 | 21:36396237 | ACTCCTGACTTGAAG[C/T]GATCTGCCTGCGTCG | 8208 |
| rs546791847 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36381554 | TACATAAATACATAG[A/G]TATGCATATATGTAA | 8208 |
| rs546828948 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CHAF1B | GRCh38.p7 | 21:36389613 | CTGTCTCAAAAAAAA[A/G]AAAAAAAAGTAAACC | 8208 |
| rs546836783 | in-del | -/ATTT | 0.00199481 | 0.0315187 | intron-variant | CHAF1B | GRCh38.p7 | 21:36405421 | AAATACATAGAGTAA[-/ATTT]ATTTATTTATTTATT | 8208 |
| rs546876263 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36394410 | AGATGGGATTTTACT[C/G]TGTTAGCCAGGCTGG | 8208 |
| rs546963169 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | MORC3 | GRCh38.p7 | 21:36375405 | AACAGACTGAAAACC[A/G]TAATCTTTACTGTAT | 8208 |
| rs546997443 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | CHAF1B | GRCh38.p7 | 21:36382381 | GAGTGGAATTGCTGA[A/G]TCATAGGGTAGGCGT | 8208 |
| rs547209014 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36388901 | CCCTGAGTAGCTGCT[C/T]GTGTTTGATCTCCCT | 8208 |
| rs547265810 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36392390 | TCCCCTTTTTCTATT[C/T]GACAAAACCGCCATC | 8208 |
| rs547562970 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36404054 | GGTTATATTTACTAA[A/C]GTTAGTTATTAAAAG | 8208 |
| rs547734789 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CHAF1B | GRCh38.p7 | 21:36398273 | TGCCCAGGCTGGTCG[C/T]GAACTGTTGAGCTCA | 8208 |
| rs547843174 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36395249 | GAGACGGGGTTTCAC[C/T]GTTGGCCAGTCTGGT | 8208 |
| rs547901182 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36412276 | GGGAAGTGCCCCAAG[C/G]TGGGCCTGTGTAGAG | 8208 |
| rs548207707 | snp | C/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36386544 | AGGAGTTTGAAGCAA[C/G]CAACGATCACTCCAC | 8208 |
| rs548209989 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36380827 | GGCTCAAGCGATGCA[C/T]TCCCCCACCTCTTAA | 8208 |
| rs548299774 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36409619 | TATTTTTACATTTAA[A/G]TCTATTTATTTATTT | 8208 |
| rs548333983 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36408985 | TCAGCCTCTTGAGTA[A/G]GTGGGATTACAGGTG | 8208 |
| rs548334311 | snp | A/G/T | 3.30803e-05 | 0.00406682 | intron-variant | CHAF1B | GRCh38.p7 | 21:36415392 | GAAATTCAGTCAGGT[A/G/T]AGTAATATTGTTACT | 8208 |
| rs548388208 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHAF1B | GRCh38.p7 | 21:36392118 | TGAGATTAGGGAGTG[A/G]TGATGACTCTGAAGG | 8208 |
| rs548421932 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36414828 | ATGTTGGTCAAGCTG[A/G]TCGAAAACTCCTGAC | 8208 |
| rs548458315 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36400128 | GTCTTAGCCGTGAGC[A/G]GAGATCATGCCACTG | 8208 |
| rs548485931 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | CHAF1B | GRCh38.p7 | 21:36404927 | TTTTGTATTTTTAGT[A/G]GAGATGGGGTTTCGC | 8208 |
| rs548498676 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36408201 | TTTTAAGTACAGCAG[G/T]GGGTGAGTGTAGAAG | 8208 |
| rs548523424 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-5-prime, upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36380164 | GCTGGGATTACAGGC[A/G]TGAGCCATCACGCCC | 8208 |
| rs548669812 | in-del | -/T | 0.0584853 | 0.160693 | intron-variant | CHAF1B | GRCh38.p7 | 21:36393263 | GAGAGGATTTTTAAA[-/T]TTTCTGTGGAGACAG | 8208 |
| rs548745048 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36392153 | TGCTGCCTTCAAGCA[A/T]CTGTTTAACAAAGCA | 8208 |
| rs548765879 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36393222 | AGCGGGAGAGGGAGA[A/G]GGAGACGGTGGAGGG | 8208 |
| rs548768762 | snp | C/G | 1.64874e-05 | 0.00287113 | intron-variant | CHAF1B | GRCh38.p7 | 21:36399501 | CTAGAAGTGGTAAAT[C/G]AGACATGTTCTTTCT | 8208 |
| rs548770379 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHAF1B | GRCh38.p7 | 21:36403903 | GAGTCCCATCCCAGC[C/T]GAGCCAGGGAGGGCC | 8208 |
| rs548895081 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36411279 | CCCCCACGCCTGGCT[A/G]ATTTTTGTATTTTTG | 8208 |
| rs548910486 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36396796 | CTCTGGGCCCTCCTC[A/G]TCTCTCTCCTGGTCT | 8208 |
| rs548958040 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36384447 | TATTATCTAAAGTAT[A/G]TAGTCATTCCCAGTC | 8208 |
| rs549018397 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36400407 | ACCTGGGAGGTGGAG[A/G]TTGCAGTGAGCTGAA | 8208 |
| rs549044005 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | CHAF1B | GRCh38.p7 | 21:36383801 | CTACAGGCGCCCGCC[A/G]CCACGCCCGACTAAT | 8208 |
| rs549062858 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36416033 | TGCTGCGATTACAGG[C/T]GTGAGCCACCGCGCC | 8208 |
| rs549124187 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36382513 | CCTGTATTGATTTCC[A/G]TCATTTCTATTTTTC | 8208 |
| rs549166781 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHAF1B | GRCh38.p7 | 21:36391167 | CTAGGGACCCTTCTG[C/T]TTAAGGTGATTTTGT | 8208 |
| rs549211938 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHAF1B | GRCh38.p7 | 21:36390247 | CTGAGGCAGGAGAAT[C/T]GCCTGAACCCGGGAG | 8208 |
| rs549212024 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36381852 | AAGAAAGCCTGTGGT[A/G]TAACTTAGTCCCACT | 8208 |
| rs549229143 | snp | A/C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | MORC3 | GRCh38.p7 | 21:36375589 | GCCCTAGAGTACTCA[A/C/G]GTGTTTTTCACCAAG | 8208 |
| rs549374297 | snp | C/T | 0.00358779 | 0.0422022 | utr-variant-3-prime | CHAF1B | GRCh38.p7 | 21:36416421 | GTGTGTGCAGGGAGA[C/T]GGTAAAGCTGGAGGT | 8208 |
| rs549394725 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | MORC3 | GRCh38.p7 | 21:36376629 | AAAAATATATGATGG[C/T]TAACTGTTCAAATGC | 8208 |
| rs549401914 | in-del | -/TTA | 0.0248475 | 0.108657 | intron-variant | CHAF1B | GRCh38.p7 | 21:36382697 | CATGCCTGGCTGTTA[-/TTA]TTATTATTATTATTA | 8208 |
| rs549518676 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CHAF1B | GRCh38.p7 | 21:36414193 | TTACCCCTCTGATCC[C/T]GTATAGTTCCTTCTC | 8208 |
| rs549608185 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36387097 | TCCTGGTTCCTACTG[A/G]GTAACAAGTTGCTCT | 8208 |
| rs549681857 | snp | C/T | 0.000199008 | 0.00997319 | intron-variant | CHAF1B | GRCh38.p7 | 21:36386274 | CAGGGTAAACTGGGG[C/T]AGAGATAGACATCCG | 8208 |
| rs549787131 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36393049 | ACCCCATCTCCACCA[A/G]AAAAATACGAAAACC | 8208 |
| rs549989116 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | CHAF1B | GRCh38.p7 | 21:36398357 | GTGATTTTTATTTTT[A/T]TTTTTTTTAAATTGT | 8208 |
| rs550105239 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36392698 | TTCTCAGACGGGGCG[G/T]CCGGGCAGAGACGCT | 8208 |
| rs550135041 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36397316 | TGCTGAGTGATGCGT[A/G]GTAAAGGGAATAATA | 8208 |
| rs550154296 | in-del | -/A | 0.121369 | 0.214369 | downstream-variant-500B | MORC3 | GRCh38.p7 | 21:36377115 | GCGAAACTCCGTCTC[-/A]AAAAAAAAAGGACTT | 8208 |
| rs550193206 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHAF1B | GRCh38.p7 | 21:36398993 | TTCAGACAGTCATCA[A/G]TAAAACAATCTGATT | 8208 |
| rs550295370 | snp | C/T | | | utr-variant-3-prime | MORC3 | GRCh38.p7 | 21:36376439 | TATGTATGCTTAATA[C/T]GTGTCGGTCATATAC | 8208 |
| rs550368917 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | CHAF1B | GRCh38.p7 | 21:36405043 | GGTGTGAGCCACTGC[A/G]CCCAGCCCCAGTAGC | 8208 |
| rs550369043 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36412769 | TTTTCCAGTTGTATC[C/T]TTTCCCTGGTTTTTG | 8208 |
| rs550517114 | snp | G/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 21:36377870 | AGTAGAATTACTTGG[G/T]GAGTTTTTTAAACTC | 8208 |
| rs550548749 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CHAF1B | GRCh38.p7 | 21:36407269 | ATCGCACCACTGCAC[C/T]CTAGCCTGGGCAACA | 8208 |
| rs550553988 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36396651 | AGAACCACACCCTGT[C/T]TCAAAAAAAAAAGAA | 8208 |
| rs550678899 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36402407 | TGCCAGTCTCAGGCC[C/T]CAGACATGCCACTAT | 8208 |
| rs550763921 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36415909 | AGGCGTGCGCCATCA[C/T]ACCCGGGTAATTTTT | 8208 |
| rs550807212 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36409730 | CTTGAACTCCTGGAC[G/T]CAAGTGATCCACCTG | 8208 |
| rs550831205 | snp | A/C | | | upstream-variant-2KB, intron-variant | CHAF1B | GRCh38.p7 | 21:36383441 | CAAATGGAAATTAAA[A/C]TGCCTTGAGAAGTTT | 8208 |
| rs550852887 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | CHAF1B | GRCh38.p7 | 21:36394336 | TGCCTCGGCCTCCCA[A/T]AGTGCTGGGATTACA | 8208 |
| rs550988091 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36399826 | AGAGCCACTGATGGA[A/G]GACAGGACAGTGGTT | 8208 |
| rs551025687 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36380908 | TTTTTTTGTTTGTTT[G/T]TTTTTCTGTACTCTG | 8208 |
| rs551069142 | snp | C/T | | | utr-variant-3-prime | CHAF1B | GRCh38.p7 | 21:36416469 | CCATGGAGCGGGACA[C/T]ACTGTAAATGGATTT | 8208 |
| rs551118475 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36385862 | CGTTTTGCTTTTCTG[C/G]ATGTAGCGGCGTATC | 8208 |
| rs551209584 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36398176 | TCATGCTTCAGCCCC[C/T]CAAGTAATTGGGACT | 8208 |
| rs551246371 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36397392 | ATGCTGTTTTGGTGC[A/G/T]TGTGTGTGTGTTTTT | 8208 |
| rs551248304 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | CHAF1B | GRCh38.p7 | 21:36404593 | GCATGCGCCACCACG[C/T]CCAGCTAATTTTGTA | 8208 |
| rs551336292 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36404005 | TGACACTTTGGCCCA[A/T]GAAGTCTCAGGACTA | 8208 |
| rs551422720 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 21:36378008 | GCCAAGCACTGTTGA[A/G]TTGTGTCTTCTGTTG | 8208 |
| rs551468802 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36384634 | TGGCTAAAAGCATCA[C/G]CCGGTATTTATATAA | 8208 |
| rs551615407 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | CHAF1B | GRCh38.p7 | 21:36416574 | ACTTGGGACATGAAC[A/G]TTTTAACGTAGTAAA | 8208 |
| rs551657765 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36402326 | CTAAAGAGTGCATTC[A/G]GTTGGAAATTCTAAT | 8208 |
| rs551659482 | in-del | -/TTTG | | | intron-variant, upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36380897 | TAGGGTTTTGTTTTT[-/TTTG]TTTGTTTGTTTTTCT | 8208 |
| rs551977010 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36414761 | GGATTACAGGCATGC[A/G]CCACCATGCCTGGCT | 8208 |
| rs551979685 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36383219 | TCAGCCTCCCTAGTA[C/T]CCCGAGTAGCTGGGA | 8208 |
| rs552051546 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHAF1B | GRCh38.p7 | 21:36416024 | CTCCCAAAGTGCTGC[A/G]ATTACAGGCGTGAGC | 8208 |
| rs552063688 | in-del | -/C | 0.00517822 | 0.0506191 | intron-variant | CHAF1B | GRCh38.p7 | 21:36391369 | TATTTTTAGTAGAGA[-/C]AGTTAGCCAGGATGG | 8208 |
| rs552115796 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36379994 | CAGGCTCAAGTGACC[C/T]CCCACCTCAGCCCCC | 8208 |
| rs552248347 | in-del | -/AT | 0.00358779 | 0.0422022 | intron-variant | CHAF1B | GRCh38.p7 | 21:36401375 | TTTATATTATACATA[-/AT]ATATATTTTTATATT | 8208 |
| rs552253023 | snp | C/T | | | utr-variant-3-prime | MORC3 | GRCh38.p7 | 21:36376234 | TTATAGTATTACATG[C/T]CATAAAATACTATGC | 8208 |
| rs552325965 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36413480 | GTCATTTCTTGCATA[C/T]AGGCCTCTGTTTGTT | 8208 |
| rs552495901 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CHAF1B | GRCh38.p7 | 21:36387230 | CATAGTTTTGTTTTT[G/T]TTTTTTTTTTGAGAC | 8208 |
| rs552513671 | in-del | -/TCCGCCT | 0.432651 | 0.170701 | intron-variant | CHAF1B | GRCh38.p7 | 21:36382620 | CTTGGCTCACTGCCC[-/TCCGCCT]TCTGGGTTCAAGTGA | 8208 |
| rs552565367 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36393836 | AATCTCATTTTAATG[C/T]TTAGTTCTGGAGATT | 8208 |
| rs552748971 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36406287 | GAGATTGGACAAAGA[A/C]CTATTCCTCTTTTTT | 8208 |
| rs552778880 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36399159 | TCTGCCTCAGCCTCC[C/T]GAGTAGCAGGGATTA | 8208 |
| rs552782034 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36400852 | GCAGGCAGCGAGGTG[C/T]GGGGAGCAAGCTGGT | 8208 |
| rs552813001 | in-del | -/A | 0.177928 | 0.239386 | intron-variant | CHAF1B | GRCh38.p7 | 21:36396654 | CCACACCCTGTCTCA[-/A]AAAAAAAAAGAAAAA | 8208 |
| rs552832808 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36412829 | ACTTCCCTCTTCTAA[C/G]TAGATGTGAGAGTGT | 8208 |
| rs552884588 | snp | A/G | | | upstream-variant-2KB, intron-variant | CHAF1B | GRCh38.p7 | 21:36384861 | ACCGACTGATTTACA[A/G]CCTCACTTTAAAATG | 8208 |
| rs553010808 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36408243 | GGGGACTGTTCCCCA[A/G]AGTGAAGTCAGGTTC | 8208 |
| rs553094544 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36414464 | TTTCTGTTTGTTTTT[A/G]TGTGACGGAAGGTAT | 8208 |
| rs553200718 | snp | C/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36405575 | GCTGGGACCACAGGC[C/G]TGTAGCACCATGCCT | 8208 |
| rs553206071 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHAF1B | GRCh38.p7 | 21:36395523 | ATCCCACATGGTGGG[A/G]CCAGCAGATAAGATG | 8208 |
| rs553265212 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36398287 | GCGAACTGTTGAGCT[C/T]AAGCCATCTGTCTGC | 8208 |
| rs553326432 | snp | G/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36400665 | AGGTCGAGCGTTGGA[G/T]CTGTCTGGCAGCAGG | 8208 |
| rs553340260 | snp | A/C/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36380407 | TCTCAAAATGTGATA[A/C/T]TCATGGAGGCAACTG | 8208 |
| rs553377667 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CHAF1B | GRCh38.p7 | 21:36388356 | CAAGGCGACTGTTCT[C/G]GTTTTGTTGGATTGT | 8208 |
| rs553716248 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CHAF1B | GRCh38.p7 | 21:36391831 | GCAGCCTTGACTTCC[C/T]GGGCTCAAGTGATCC | 8208 |
| rs553736700 | in-del | -/T | 0.00478085 | 0.0486577 | intron-variant | CHAF1B | GRCh38.p7 | 21:36391870 | CCAAATAGCTGGGAC[-/T]TACAGGTGCATGCTA | 8208 |
| rs553745640 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36405560 | TCAGCCTCCCTACTA[A/G]CTGGGACCACAGGCG | 8208 |
| rs553852738 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | CHAF1B | GRCh38.p7 | 21:36383687 | AGAGTCTCGCTCTCT[C/T]GCCCAGGCTGGAGTG | 8208 |
| rs553853906 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36393962 | TGGAGTGCAGTGGCA[C/T]GATCTTGGCTCACTG | 8208 |
| rs553978547 | snp | A/G | | | intron-variant, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36381648 | TTTCTGTGTTTGCCA[A/G]TCACTTGAAATAATA | 8208 |
| rs554019032 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CHAF1B | GRCh38.p7 | 21:36383949 | TACCGCGACCGGCAG[G/T]AATTCTTTAGTCCAA | 8208 |
| rs554114426 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36389059 | GCCGGTCGGGGTAAG[A/G]TCCCGCGTCGGTACC | 8208 |
| rs554270648 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36403392 | AACCCAGGAGGCAGA[A/G]GGTGCAGTGAGCCGA | 8208 |
| rs554361437 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CHAF1B | GRCh38.p7 | 21:36394177 | TGCCTCCCAGGTTCA[A/G]GTGATTCCCCTCCCT | 8208 |
| rs554362524 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36411393 | TGCTGGGATTCTAGG[C/T]GTGAGCCATTGCACC | 8208 |
| rs554821268 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36408488 | CCTATGGCAAAGGCT[C/T]ACTATGTTCTCCTCG | 8208 |
| rs554955532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36399195 | GCCCACCACCACGCC[C/T]GGCTAATTTTTTGTA | 8208 |
| rs554985092 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CHAF1B | GRCh38.p7 | 21:36386377 | CCTGTAATCCCAGTG[C/G]TTTGGGAGGCTGAGG | 8208 |
| rs554994032 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36406447 | CCGGCCACCATGCCC[A/C]GCTAATTTTTGTATT | 8208 |
| rs555000640 | snp | C/G | | | | | GRCh38.p7 | 21:36377649 | CTAGGGTGGCAAAAT[C/G]AGTGAAAGCTGAGTG | 8208 |
| rs555063339 | snp | A/T | | | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36379357 | TCGCCATGTCCAGGC[A/T]GGTCTTAAGCTCCTG | 8208 |
| rs555085375 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36387312 | AGTGCAGCCCCGACC[C/T]GGGGCTCAAGTGATC | 8208 |
| rs555205898 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36392805 | ACTCACTTCCTAGAC[A/G]GGGTGGCGGCCGGGC | 8208 |
| rs555274835 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36398519 | TGTGTACCACCATGC[C/T]TGGCTAATTTTTGTA | 8208 |
| rs555294026 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CHAF1B | GRCh38.p7 | 21:36392513 | GGCCGGGCAGAGGCG[C/T]CCCCCACCTCCCGGA | 8208 |
| rs555316782 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36397888 | ACATGCCACCATGCC[C/T]GGTTAATTTTTGTGT | 8208 |
| rs555322642 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36415020 | AGTGTTCACAAGACC[A/G]TCGGTAATGAACAGA | 8208 |
| rs555366765 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | CHAF1B | GRCh38.p7 | 21:36416672 | CTCCCTGGCATCCTC[A/G]TGAAAGTGCACACAC | 8208 |
| rs555475250 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36409202 | GATGGGGTTTCGTCA[A/T]GTTGGCCAGGCTGGT | 8208 |
| rs555484512 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36402019 | GTGCTGGGATTACAG[G/T]TGTGAGCCACCATGT | 8208 |
| rs555508965 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36381895 | GAACCAGGGACACCA[G/T]TGGCATAAGTCCTGG | 8208 |
| rs555571234 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CHAF1B | GRCh38.p7 | 21:36382857 | GATTACAGGTGCCTG[C/T]CACCGCGCCTGACCT | 8208 |
| rs555622899 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36381087 | CATTGTTTCTAGTTA[A/G]GCCATTTCTTTTTCT | 8208 |
| rs555644889 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CHAF1B | GRCh38.p7 | 21:36390520 | AATGGGTGACCTCAG[C/G]CTAAAGTACCTGATA | 8208 |
| rs555652853 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36396767 | CCCTTTTCCATCCCT[A/G]TTCGCATTGTCTGCT | 8208 |
| rs555711299 | snp | G/T | 1.64746e-05 | 0.00287002 | missense | CHAF1B | GRCh38.p7 | 21:36399541 | TGCGAGTATACAGTA[G/T]ACAGAAGAAGCGTGT | 8208 |
| rs555748091 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | CHAF1B | GRCh38.p7 | 21:36407354 | TTGCAAGCATTGTTT[A/T]TAGTGGTAAAAAACC | 8208 |
| rs555748285 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CHAF1B | GRCh38.p7 | 21:36399274 | CTCCTGACCTCAAGT[A/G]ATTCACCCGCCTCTG | 8208 |
| rs555964894 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36412508 | GGGATTACAGGCGCC[C/T]ACCACCATGGCTGGC | 8208 |
| rs556056463 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36378361 | CATTTCATCATAGGA[A/G]TATGCTCCTAATGGT | 8208 |
| rs556095039 | snp | C/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 21:36377560 | ACAGTATTGCTTCAA[C/G]TAATGTTTATTACTT | 8208 |
| rs556095855 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CHAF1B | GRCh38.p7 | 21:36392887 | GGAGGTTGTAGCGAG[C/T]GGAGACCACGCCAGT | 8208 |
| rs556181176 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36384193 | AATCCACAGTTCAGA[A/G]TCGTGACACTTCAAG | 8208 |
| rs556603225 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36392000 | CAGGGTCATAGGACA[A/G]TAGTGGAGGGAAGGT | 8208 |
| rs556689012 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36397698 | GACAAGTGCCTTACA[C/T]GAAGTTTGTACTTAG | 8208 |
| rs556801948 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CHAF1B | GRCh38.p7 | 21:36404208 | CAGTTTCAAGCGATT[C/G]TCCTGCCTCAGCCTC | 8208 |
| rs556849617 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CHAF1B | GRCh38.p7 | 21:36394710 | CATCTATAAAAGCCT[A/G]AAAGTCTAACTTGCT | 8208 |
| rs556889961 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CHAF1B | GRCh38.p7 | 21:36403501 | TTTACTATTTAAACC[C/T]TTTCAATGAATGCTT | 8208 |
| rs556956973 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | CHAF1B | GRCh38.p7 | 21:36389832 | TTGTAGAGGGAAAAG[G/T]GGGGAGCAGGAGCGC | 8208 |
| rs557053406 | snp | A/G | 0.0023933 | 0.0345097 | | | GRCh38.p7 | 21:36377790 | TTCTTGCTGTCACAT[A/G]AGACGTCTTAAACTT | 8208 |
| rs557100342 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36414409 | CGCCCTCTTAAAATC[G/T]CTCATTTCTTTCTGC | 8208 |
| rs557244890 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CHAF1B | GRCh38.p7 | 21:36404982 | CTCCTGACCTCAGGT[A/G]ATCTGCCCACCTTGG | 8208 |
| rs557253087 | snp | C/T | | | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36379864 | AATTTGGCTGTAGTT[C/T]GTTTTTTTTTTTTTT | 8208 |
| rs557260022 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CHAF1B | GRCh38.p7 | 21:36414916 | TCTTGCCCGGCCCAA[C/T]GCTCTGGATTTTAAA | 8208 |
| rs557289949 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36400472 | GCGAAACTCAGTCTC[A/T]AAATAAATAAATAAA | 8208 |
| rs557313510 | snp | G/T | 0 | 0 | intron-variant | CHAF1B | GRCh38.p7 | 21:36387529 | CCCAGCCCATAGTAT[G/T]GTTTTAATACAGACA | 8208 |
| rs557369042 | snp | A/G | | | downstream-variant-500B | MORC3 | GRCh38.p7 | 21:36376854 | GGCGCAGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 8208 |
| rs557387006 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36413854 | CTCCAGTTCCCCTGC[C/T]GGTTGTGAGCCCCCA | 8208 |
| rs557484889 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36388154 | TTCAGGTGTGGCTGA[C/T]CCTCTCAATCTGTCA | 8208 |
| rs557506235 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36380264 | CTCCCATGGGGTTCC[G/T]GTTGGAAGTGAGGCT | 8208 |
| rs557572707 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36411191 | CAATCTGAGCTCACT[A/G]CAACCTCCGCCTCCT | 8208 |
| rs557610606 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | CHAF1B | GRCh38.p7 | 21:36416867 | AGGTGACGATGCTTA[C/T]TCTTTTAGTAACTAA | 8208 |
| rs557666812 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36386658 | ACTTTGTCATCTAGC[C/T]CAGAATGCTAAATTT | 8208 |
| rs557742980 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36396458 | TCAAGCCTAGGAATT[C/T]AAGACCAGCATGGGC | 8208 |
| rs557749963 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36411940 | CGCCCTGTTGGCCAG[A/G]CTGGTATCAAACTCC | 8208 |
| rs557840441 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CHAF1B | GRCh38.p7 | 21:36390664 | TAGATATATTGTTAT[C/T]CTCATTTTTGAGACA | 8208 |
| rs558018601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36391276 | TTGGAAGTAAATCAT[C/T]CTGGCCATAGTGTCC | 8208 |
| rs558091678 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | CHAF1B | GRCh38.p7 | 21:36410002 | GGGGTCTTGCTCTGT[C/T]GCCCAGGCTGGAGTG | 8208 |
| rs558128216 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHAF1B | GRCh38.p7 | 21:36415696 | AGGACTGTCCTGTGT[A/G]TTATGCGATGTTTAA | 8208 |
| rs558217922 | snp | A/G | 0.00044778 | 0.0149562 | intron-variant | CHAF1B | GRCh38.p7 | 21:36399657 | TTAACTGAGACTTAG[A/G]AAGTCATGAGCTCCT | 8208 |
| rs558223633 | snp | C/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36401240 | CCATTGCACTCCAGC[C/G]TGGGCAACAAGAGCG | 8208 |
| rs558395919 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36407407 | AACAGAGGCTGGGTG[A/C]ATGAATCTTGCAGTA | 8208 |
| rs558566400 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36378421 | AATATACTGGCTGGG[C/T]GCAGTGGCTCGTGCC | 8208 |
| rs558570635 | in-del | -/CCT | 0.00636936 | 0.0560724 | intron-variant | CHAF1B | GRCh38.p7 | 21:36409249 | CAGGTGATCCGCCTG[-/CCT]CCTCCTCCCAAAGTG | 8208 |
| rs558721039 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36386493 | GCTGTAGGCCCAGCT[A/G]CTTGGGAAGTTGAAG | 8208 |
| rs558985033 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CHAF1B | GRCh38.p7 | 21:36385254 | CGACCCCAGGGCCAG[A/G]GCAGGACTCGCCTTG | 8208 |
| rs559064543 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CHAF1B | GRCh38.p7 | 21:36409537 | GTGGGGTGGAGATTT[C/G]GATTCTGTCTTATGG | 8208 |
| rs559080795 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CHAF1B | GRCh38.p7 | 21:36392737 | CCCAGACAGGGCGGC[C/G]GGGCAGAGGCGCTCC | 8208 |
| rs559206721 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36398401 | ATCTCACTCTGTCAC[C/T]CTGGCTGGAATGCAG | 8208 |
| rs559255958 | snp | C/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36390053 | AGCATGGGAATGCAG[C/G]CTGGGTGCGGTGGCT | 8208 |
| rs559294617 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36380754 | GCCCAGCTAATTTTC[A/G]TATTTTTTGTGGAGA | 8208 |
| rs559320432 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | CHAF1B | GRCh38.p7 | 21:36404412 | CCCTTTTTTTTTTTT[A/T]AAATTATTTATTTTA | 8208 |
| rs559384135 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36388628 | CCTGCCACCACCCCC[G/T]GCTAATTTTTGTATT | 8208 |
| rs559473236 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36381258 | CCCAAGTACCTGGGA[C/T]TATAGGTGCATGCCA | 8208 |
| rs559598605 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36389348 | TCGCTCACACATGTT[A/G]TAATCCCAGCACTTT | 8208 |
| rs559633404 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36407853 | CATCGTGGCAGGTGC[C/G]TGTAATCCCGGCTAC | 8208 |
| rs559694283 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36403069 | GGTCTGGGTGGCCTG[A/G]CTTTTGGAATTTTAA | 8208 |
| rs559713022 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | CHAF1B | GRCh38.p7 | 21:36394297 | GGCCAGGATGGTCTC[C/G]ATCTCCCGACCTTGT | 8208 |
| rs559753151 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36408672 | AAGTATTTTGCAAAC[C/T]GGACCTGAAGGCTCT | 8208 |
| rs559817490 | in-del | -/GTAA | 0.00159617 | 0.0282053 | intron-variant | CHAF1B | GRCh38.p7 | 21:36390597 | GCCAGCCATTGTGTT[-/GTAA]GTGTGTTATATACAT | 8208 |
| rs559839752 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CHAF1B | GRCh38.p7 | 21:36399991 | TGAGACCAGCCTGGC[A/C]AACATGGCCAAACCC | 8208 |
| rs559900579 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36415838 | GCTCACTGCAGCCTC[C/T]ACCTCCCACGTTCAA | 8208 |
| rs559974376 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36411216 | CCTCCTGGGTTCAAG[C/T]GATTCTCCTGTCTCA | 8208 |
| rs559981622 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | CHAF1B | GRCh38.p7 | 21:36417019 | TTTATTTCATATGCA[A/G]TTTGGTATCTAAATA | 8208 |
| rs559982848 | snp | C/T | 0.00517822 | 0.0506191 | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36379631 | TTTAGAATTGTCTAT[C/T]GATCACAGAGTTAAC | 8208 |
| rs559989848 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36413777 | CTCTGTTTGCAGTCT[C/T]TGTGGCCCTTCAGCC | 8208 |
| rs559998758 | snp | C/G | | | upstream-variant-2KB, intron-variant | CHAF1B | GRCh38.p7 | 21:36384070 | CCGCATCCCCTGCCC[C/G]TGTTGGCTCATCAAG | 8208 |
| rs560087735 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36380466 | TTGCTTGGTTGTGTT[G/T]TTTTAGTTTTTTTTC | 8208 |
| rs560094756 | snp | C/T | 0.000188293 | 0.00970109 | missense | CHAF1B | GRCh38.p7 | 21:36416278 | TTAATGTTGCAGAGA[C/T]GCCTGGAGACGCTCA | 8208 |
| rs560205066 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36390848 | TTTAGTAGAGACAAG[A/G/T]TCTTGCTCTCTTGCC | 8208 |
| rs560209586 | snp | A/G | 4.99571e-05 | 0.00499761 | intron-variant | CHAF1B | GRCh38.p7 | 21:36391521 | GAGTGTGGGTGAAGC[A/G]TGGATCACTGTTACT | 8208 |
| rs560236601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36403817 | GTGGCTCCAGGACCA[C/T]CCTGTGCATAGAGAT | 8208 |
| rs560241448 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36396519 | AATACAAAAATTAGC[C/T]GGGTGTGGTAGTACA | 8208 |
| rs560315624 | snp | A/G | 0.0023933 | 0.0345097 | downstream-variant-500B | MORC3 | GRCh38.p7 | 21:36376778 | TTCCATTAAGACTGA[A/G]GCTGAGCTCCTCTTT | 8208 |
| rs560330390 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36396014 | TGTGGTTTTTTTTTT[C/T]ATTTTAGATGGAGTC | 8208 |
| rs560379066 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHAF1B | GRCh38.p7 | 21:36382409 | CGTATCATTAACTTT[A/G]TTAGACAGTGCTGAA | 8208 |
| rs560413988 | in-del | -/G | 0.00279162 | 0.0372561 | intron-variant | CHAF1B | GRCh38.p7 | 21:36400446 | ATTGCACTCCAGCCT[-/G]GGTGACAAGAGCGAA | 8208 |
| rs560543070 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36389954 | TGCTGTTGTCAGCAC[A/G]TGGAGAGTGTTCATC | 8208 |
| rs560546466 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CHAF1B | GRCh38.p7 | 21:36383125 | ACAGAATCTCACTCT[G/T]CCACCCAGGCTGGAG | 8208 |
| rs560664774 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CHAF1B | GRCh38.p7 | 21:36401443 | TATTTTTATATTATA[C/T]ATAATATATATTTTT | 8208 |
| rs560681279 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36393626 | CCAGCTAATTTTTTT[C/G]TATTTTTAGTAGAGA | 8208 |
| rs560707331 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36406442 | AGGCGCCGGCCACCA[C/T]GCCCAGCTAATTTTT | 8208 |
| rs560754636 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | CHAF1B | GRCh38.p7 | 21:36393013 | TTAGGAGCTGGAGAC[C/G]AGCCCGGCCAACACA | 8208 |
| rs560761896 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36382861 | ACAGGTGCCTGCCAC[C/T]GCGCCTGACCTATTT | 8208 |
| rs560881867 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CHAF1B | GRCh38.p7 | 21:36410022 | AGGCTGGAGTGCAGT[G/T]GTGCAATCTTGGCTC | 8208 |
| rs561018567 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36379290 | TAGCTGGCACTAGAG[G/T]CGTGCACCACCATGC | 8208 |
| rs561019426 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36399321 | GATTACAGGCGTGAG[C/T]TACCGCGCCCGGCCT | 8208 |
| rs561060794 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36407048 | GGCTCAAGCCTGTAA[C/T]CCCAGCACTCTGGGA | 8208 |
| rs561287666 | snp | C/T | 1.79612e-05 | 0.00299671 | missense | CHAF1B | GRCh38.p7 | 21:36413311 | TGGAGCAAGACAACA[C/T]CCCGGTAAGAACTTG | 8208 |
| rs561356738 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36406054 | ATATGGTGTTGCTAT[A/C]GGACCAAACAAATAG | 8208 |
| rs561475401 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-5-prime, intron-variant | CHAF1B | GRCh38.p7 | 21:36385422 | CTGCGCGGGAGGTGA[C/T]GGTGCCTCTGACTGT | 8208 |
| rs561562934 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36384414 | TAGGGCCAGGAATCT[C/G]TACTTTTAGAACAGC | 8208 |
| rs561686872 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36410895 | CGAACTCCTGACCTC[A/T]GGTGATCTGCCCGCC | 8208 |
| rs561689307 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CHAF1B | GRCh38.p7 | 21:36402348 | AATTCTAATGAATCC[A/G]CACAGATAGAAAGCA | 8208 |
| rs561729260 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36410156 | TTAGTAGAGATGGGA[G/T]TTTGCCATGTTGGCC | 8208 |
| rs561851658 | snp | C/T | 1.65449e-05 | 0.00287614 | intron-variant | CHAF1B | GRCh38.p7 | 21:36415395 | ATTCAGTCAGGTAAG[C/T]AATATTGTTACTGGT | 8208 |
| rs561865837 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36415888 | CTCCCGAGTAGCCGG[C/G]ACTACAGGCGTGCGC | 8208 |
| rs561876449 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | MORC3 | GRCh38.p7 | 21:36375088 | TACTTTTTAAGGTCT[A/G]CATGAATCTTAACTT | 8208 |
| rs561924822 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CHAF1B | GRCh38.p7 | 21:36390265 | CTGAACCCGGGAGGC[A/G]AAGGTTGTGGTGAGC | 8208 |
| rs561925298 | in-del | -/GCTGT | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36397938 | CACCACGTTGGTCAA[-/GCTGT]GCTGTTCTCAAACTC | 8208 |
| rs561944089 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36381301 | GATTTTTTTTTTTTT[C/T]TTCTAGATACGGAGT | 8208 |
| rs562002396 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36408333 | AGGGAAGTTGGGGAA[A/C]GGCGAGTCTCAGCCT | 8208 |
| rs562038519 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36394326 | GTGATCTGCCTGCCT[C/T]GGCCTCCCAAAGTGC | 8208 |
| rs562067497 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36388747 | GCTAGGATTACAGGC[A/G]TGAGCCACCGCGCCC | 8208 |
| rs562075255 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36400659 | ACAGGCAGGTCGAGC[A/G]TTGGATCTGTCTGGC | 8208 |
| rs562204956 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36401088 | CCTGGCTAACATGGT[A/G]AAACCCTGTCTCTAC | 8208 |
| rs562354838 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHAF1B | GRCh38.p7 | 21:36392547 | GGCAGCTGGCCGGGC[A/G]GGGGCTGCCCCCCAC | 8208 |
| rs562367467 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | CHAF1B | GRCh38.p7 | 21:36404559 | CCTGCCTCAGCCTCC[A/G]GAGTAGCTGGGATTA | 8208 |
| rs562402834 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36403929 | GGGCCTGAGAAGGGC[A/G]TGAATCACACATGCA | 8208 |
| rs562404925 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CHAF1B | GRCh38.p7 | 21:36412020 | GGCGTGAGCCACCAC[A/G]CCCGGCCCCAATTTT | 8208 |
| rs562411924 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36415547 | CGGCTGCCTGTTTAC[A/G]CCTCAGCAGGGGGCA | 8208 |
| rs562433130 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CHAF1B | GRCh38.p7 | 21:36385505 | TGGTCGCGTCGGTCC[A/G]GGCCAGAGGCCCTCG | 8208 |
| rs562442608 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36398619 | CCTGCGTTGGCCTCC[C/T]AAAGTGCTGGGATTA | 8208 |
| rs562457790 | in-del | -/T | 0.00517822 | 0.0506191 | intron-variant | CHAF1B | GRCh38.p7 | 21:36401406 | TATACATAATATATA[-/T]TTTTATATTATACAT | 8208 |
| rs562490827 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CHAF1B | GRCh38.p7 | 21:36411739 | TTTTGTTTCTTATTT[A/T]TTTTTTTGAGACCAA | 8208 |
| rs562505011 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | CHAF1B | GRCh38.p7 | 21:36393005 | ACTCGCGATTAGGAG[C/T]TGGAGACCAGCCCGG | 8208 |
| rs562584654 | snp | A/T | 0.000399281 | 0.0141238 | downstream-variant-500B | MORC3 | GRCh38.p7 | 21:36377144 | TTTTCTTTGTATAAA[A/T]CATTTACTCTAGAGA | 8208 |
| rs562600867 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36392179 | AAGCACATCTTGTAC[C/T]GTCCTTAATCCATTT | 8208 |
| rs562621383 | snp | C/G/T | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | CHAF1B | GRCh38.p7 | 21:36383734 | GCTCACTGCAAGCCC[C/G/T]GCTTCCCGGGTTCAC | 8208 |
| rs562637118 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36398033 | CCCGCCCTGAACTTA[A/G]TAAATCTTTATTATT | 8208 |
| rs562708595 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHAF1B | GRCh38.p7 | 21:36413406 | AGGTGAAATTTCAGG[C/T]GGTGAATGCTTCATG | 8208 |
| rs562769843 | snp | A/G | | | utr-variant-3-prime | CHAF1B | GRCh38.p7 | 21:36416568 | TTTTTAACTTGGGAC[A/G]TGAACGTTTTAACGT | 8208 |
| rs562883028 | snp | C/T | 0.00159617 | 0.0282053 | downstream-variant-500B | CHAF1B | GRCh38.p7 | 21:36417155 | CAGCTCACTGCAGCC[C/T]CGACCTCCTGGGCTC | 8208 |
| rs562946530 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36393081 | GACAGGCGTGGCGGC[A/G]TGCGCCTGCAATCCC | 8208 |
| rs563106126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36390960 | CCCACCCTGCCTATT[A/G]TCCCCATTTACAGGT | 8208 |
| rs563338845 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHAF1B | GRCh38.p7 | 21:36387905 | CTCACTGCAACCTCC[A/G]CCTCCTGGGTTCAAG | 8208 |
| rs563433907 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36393746 | GGCGTGAGCCACTGC[A/G]ACCGGTCAGATATAG | 8208 |
| rs563461895 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CHAF1B | GRCh38.p7 | 21:36388586 | ATTCTCCTGCCTCAG[C/T]CTCACAAGTAGCTGG | 8208 |
| rs563609395 | snp | A/G | | | intron-variant, upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36380944 | TCCAGGGTATTTCAG[A/G]TGTAAGGTATTTCAA | 8208 |
| rs563612028 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36399900 | AATATGGGTGCTGGC[C/T]GGGCGCCGTGGCTCA | 8208 |
| rs563637098 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHAF1B | GRCh38.p7 | 21:36393054 | ATCTCCACCAAAAAA[A/G]TACGAAAACCAGACA | 8208 |
| rs563694847 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36407775 | TTGAGGTCAGGAGTT[C/T]GAGACCACCCTGGCC | 8208 |
| rs563696905 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36399331 | GTGAGCTACCGCGCC[C/T]GGCCTGTAATATCCT | 8208 |
| rs563733536 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36407163 | AAAAATTAGCCGGGC[A/T]TGGTGATGCACACCT | 8208 |
| rs563883929 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36412794 | TTTTTGCCTTCAAAC[A/G]AGCTTGTGATTTTGC | 8208 |
| rs563914962 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36379045 | TGTAAAGAAGCTGAA[A/G]GCTTGTGTTAATTTG | 8208 |
| rs564121264 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CHAF1B | GRCh38.p7 | 21:36402964 | AGAGTGGGGGTCCCC[A/G]ACTTACCTGCCCATT | 8208 |
| rs564193488 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36415912 | CGTGCGCCATCACAC[C/T]CGGGTAATTTTTGTA | 8208 |
| rs564201616 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36382960 | TGATCCGCCCGCTTC[A/T]GCCTCCCAGATGCTG | 8208 |
| rs564240100 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | CHAF1B | GRCh38.p7 | 21:36396003 | GTCTTGTTTTGTGTG[G/T]TTTTTTTTTTTATTT | 8208 |
| rs564244804 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36411116 | ATTCTTATAAATATT[A/C]TTTTTTTTTTTTTTT | 8208 |
| rs564266518 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36395009 | GTGCTGGGATTACAG[A/G]CATGAACCACTGCCC | 8208 |
| rs564287319 | snp | A/C/T | 5.04964e-05 | 0.00502455 | missense | CHAF1B | GRCh38.p7 | 21:36416325 | CTAAAGCGGCCCAGA[A/C/T]TCGATGAAAACAAAG | 8208 |
| rs564350034 | snp | A/G | 1.66164e-05 | 0.00288235 | missense | MORC3 | GRCh38.p7 | 21:36375291 | AGTGAAATCAGTAGT[A/G]CTTAAAGTATATGTT | 8208 |
| rs564390099 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CHAF1B | GRCh38.p7 | 21:36400715 | GTAGGTAGAGAGTTT[C/T]GCTAGCAGACAGCAG | 8208 |
| rs564457321 | snp | A/G | | | utr-variant-3-prime | MORC3 | GRCh38.p7 | 21:36376246 | ATGCCATAAAATACT[A/G]TGCTTTATTGGTCCC | 8208 |
| rs564506271 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36390066 | AGGCTGGGTGCGGTG[C/G]CTCACGCCTGTAATC | 8208 |
| rs564518859 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36378453 | GTAATCCCAGCACTT[C/T]GGGAGGCCAAGGTGG | 8208 |
| rs564627033 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CHAF1B | GRCh38.p7 | 21:36392995 | CTGGCAGATCACTCG[C/T]GATTAGGAGCTGGAG | 8208 |
| rs564666073 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CHAF1B | GRCh38.p7 | 21:36392616 | TCTTCCCAGACGGGG[C/T]GGCTGCTGGGCGGAG | 8208 |
| rs564666320 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36399283 | TCAAGTGATTCACCC[G/T]CCTCTGCCTCCCAAA | 8208 |
| rs564698085 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36379130 | GAAAATCCACAGTAG[G/T]TTGTCTTTTTTTTTT | 8208 |
| rs564753256 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36409243 | TGACCTCAGGTGATC[C/T]GCCTGCCTCCTCCTC | 8208 |
| rs564839140 | snp | C/T | 1.71944e-05 | 0.00293205 | intron-variant | CHAF1B | GRCh38.p7 | 21:36415250 | AAACAATTCCTGTGA[C/T]ACTAATGAGCCATCA | 8208 |
| rs564860683 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36385643 | TCCCAGCTTCCCGGG[C/T]CCAGCGCCCGGTCCC | 8208 |
| rs564938705 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36416044 | CAGGCGTGAGCCACC[A/G]CGCCCAGCTTGCCCA | 8208 |
| rs565070140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36412641 | TGCTGGGATTACAGG[C/T]GTGAGCCACCGCACC | 8208 |
| rs565111656 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 21:36377253 | GGAATTTGCTATTTT[C/T]CCCTTCCTTTTGGCC | 8208 |
| rs565222338 | snp | C/T | 0 | 0 | intron-variant | CHAF1B | GRCh38.p7 | 21:36404660 | TCTGGTCTCGAACTC[C/T]GGACCTCAGGTGATC | 8208 |
| rs565337306 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36392039 | AAACAAGTGAACAAG[C/G]GTCTCTGGTTTTCCT | 8208 |
| rs565337756 | in-del | -/T | 0.000720974 | 0.0189728 | intron-variant | CHAF1B | GRCh38.p7 | 21:36397402 | GTGCGTGTGTGTGTG[-/T]TTTTTTTTGTAGGAC | 8208 |
| rs565486320 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CHAF1B | GRCh38.p7 | 21:36383756 | CGGGTTCACGCCATT[C/G]TCTTGCCTCAGCCTC | 8208 |
| rs565597013 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHAF1B | GRCh38.p7 | 21:36400410 | TGGGAGGTGGAGGTT[A/G]CAGTGAGCTGAAATC | 8208 |
| rs565650465 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36400790 | ACTTTCAAATAATTG[A/G]CAAATGAAAATAGGA | 8208 |
| rs565661556 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36400630 | GGGAAGATCCCTACA[C/T]GAGGCAACAGAAGAC | 8208 |
| rs565683992 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36408453 | TTCAATCGAGGAATT[C/G]CCTGGAGGCTCAACG | 8208 |
| rs565736051 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHAF1B | GRCh38.p7 | 21:36408917 | TGGAGTGCAATGGTG[C/T]GATCTCTGCTCACTG | 8208 |
| rs565864661 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CHAF1B | GRCh38.p7 | 21:36414278 | GGAAGGGGGATGCAG[A/G]GGGGAGTGGTGGGGA | 8208 |
| rs565998800 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CHAF1B | GRCh38.p7 | 21:36387979 | GCCTGCCACCACGCC[C/T]GGCTAGTTTTTTTGT | 8208 |
| rs566132460 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36393078 | CCAGACAGGCGTGGC[A/G]GCGTGCGCCTGCAAT | 8208 |
| rs566208902 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CHAF1B | GRCh38.p7 | 21:36406324 | GGGTTTCACCCTTGT[C/T]GCCCAGGCTTGAGAG | 8208 |
| rs566216914 | snp | A/G | | | downstream-variant-500B | MORC3 | GRCh38.p7 | 21:36376842 | TTTTCTCAGCCTGGC[A/G]CAGTGGCTCACGCCT | 8208 |
| rs566218281 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36399431 | GCTGAAAACTGTTGC[A/G]GTGGTAATAGGCTGT | 8208 |
| rs566220201 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | CHAF1B | GRCh38.p7 | 21:36392776 | CAGACGATGGGCGGC[C/T]GGGCAGAGACGCTAC | 8208 |
| rs566248586 | snp | A/C/T | 3.63579e-05 | 0.00426355 | intron-variant | CHAF1B | GRCh38.p7 | 21:36412833 | CCCTCTTCTAAGTAG[A/C/T]TGTGAGAGTGTTGGT | 8208 |
| rs566251616 | in-del | -/ACTT | | | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36378894 | CTCAAAGTCTCTCAA[-/ACTT]ACTTTTGCTAATTTG | 8208 |
| rs566258301 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36399179 | AGCAGGGATTACAGG[C/T]GCCCACCACCACGCC | 8208 |
| rs566376439 | snp | A/C | | | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36378180 | TCTCCACGGCCTCTA[A/C]AGGTAACCACTATTG | 8208 |
| rs566469393 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | CHAF1B | GRCh38.p7 | 21:36383366 | CTCCCAAAGCGTTGG[A/G]ATTATAGATGTGAGC | 8208 |
| rs566513584 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36416015 | CGCCTCAGCCTCCCA[A/G]AGTGCTGCGATTACA | 8208 |
| rs566571560 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36402996 | GAACCTCCAGGAGAG[C/T]TTCAAAAAACACATT | 8208 |
| rs566692589 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHAF1B | GRCh38.p7 | 21:36396276 | AAGTGCTGGGATTAC[A/G]GGCATGAGCCATTGC | 8208 |
| rs566723344 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHAF1B | GRCh38.p7 | 21:36386549 | TTTGAAGCAAGCAAC[A/G]ATCACTCCACTGCAC | 8208 |
| rs566743353 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CHAF1B | GRCh38.p7 | 21:36389640 | AACCTTTTTACCATA[C/T]TTTAAAACAATCTAG | 8208 |
| rs566866798 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36394436 | GCTGGCCTTGAACTC[C/G]TGACCACAGGCAGTC | 8208 |
| rs566909599 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CHAF1B | GRCh38.p7 | 21:36406470 | TTTGTATTTTTAGTA[C/G]AGATGAGGTTTTACC | 8208 |
| rs566911375 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36413583 | TGTCATCCAGGACTG[C/T]GGCCACTCTCTCTCC | 8208 |
| rs566995930 | snp | C/T | 3.33006e-05 | 0.00408034 | missense | CHAF1B | GRCh38.p7 | 21:36413125 | CCCGGCACGACTCCC[C/T]CTCAGGCCAGACAGG | 8208 |
| rs567055933 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36392297 | TTTCTTAGTACAGAA[C/T]AAAATGGAGTCTCCT | 8208 |
| rs567058820 | snp | A/G | | | downstream-variant-500B | CHAF1B | GRCh38.p7 | 21:36417265 | CATGCACCCACACAC[A/G]CACATATATATGATA | 8208 |
| rs567214284 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CHAF1B | GRCh38.p7 | 21:36384841 | TGAGGTATCTATCTC[C/T]GCCTACCGACTGATT | 8208 |
| rs567215357 | snp | C/G | | | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36379419 | AAATTGTTGGGATTA[C/G]AGGCATTTGAGCCAC | 8208 |
| rs567218099 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36392667 | GGGGCGGCTGCCGGG[C/T]GGAGGGGCTCCTCAC | 8208 |
| rs567231249 | snp | A/G | | | intron-variant, upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36381260 | CAAGTACCTGGGACT[A/G]TAGGTGCATGCCACC | 8208 |
| rs567317252 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36378754 | TAAATCCAGAGTGTA[A/C]ATTGTTAACAGTGAA | 8208 |
| rs567335103 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36410108 | GCTGGGATTACAGGC[A/G]CATGCCACCACACCC | 8208 |
| rs567552283 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36408198 | CTGTTTTAAGTACAG[C/T]AGGGGGTGAGTGTAG | 8208 |
| rs567572446 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36398302 | CAAGCCATCTGTCTG[C/T]CTTGGCCACCCAAAG | 8208 |
| rs567608777 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHAF1B | GRCh38.p7 | 21:36404978 | CAAACTCCTGACCTC[A/G]GGTGATCTGCCCACC | 8208 |
| rs567643102 | snp | A/G | | | intron-variant, upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36380932 | TACTCTGTATACTCC[A/G]GGGTATTTCAGATGT | 8208 |
| rs567841627 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36411875 | CTGGGATTACAGGTG[C/T]GCACCACTACGCCTG | 8208 |
| rs567857624 | snp | C/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 21:36377276 | TTTTGGCCAGCTTCT[C/G]TATGTATTCTTGCAA | 8208 |
| rs567967052 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | CHAF1B | GRCh38.p7 | 21:36416654 | TGTGAAAATCAGTGA[C/G]TCCTCCCTGGCATCC | 8208 |
| rs567991669 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CHAF1B | GRCh38.p7 | 21:36383768 | ATTGTCTTGCCTCAG[C/T]CTCCCGAGTAGCTGG | 8208 |
| rs568032202 | in-del | -/T | 0.147991 | 0.228242 | intron-variant | CHAF1B | GRCh38.p7 | 21:36404399 | CACCACGCCCGGCCC[-/T]TTTTTTTTTTTTTAA | 8208 |
| rs568071824 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CHAF1B | GRCh38.p7 | 21:36395294 | CTCAGGTGATCCACC[C/G]GCCTCGGCCTCCCAA | 8208 |
| rs568108591 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36401915 | TTAGATAATTTTTGT[A/T]TTTTTAGTAGAGATG | 8208 |
| rs568109826 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36400841 | AGGCTACCGAGGCAG[A/G]CAGCGAGGTGCGGGG | 8208 |
| rs568111226 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36407216 | CTGAGGCAGGAGAAT[C/T]GCTCCAACCCAGGAG | 8208 |
| rs568210619 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36409690 | TTTGGTAGCGACAGC[A/G]TTTCACCATGTTGCC | 8208 |
| rs568247081 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36409003 | GGGATTACAGGTGCC[C/T]GCCACCACTCCTAGT | 8208 |
| rs568383390 | snp | G/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36405694 | CCTCGGCCTCCCAAA[G/T]AGCTGGGATTACAGG | 8208 |
| rs568463144 | snp | A/T | 0.0267878 | 0.112589 | intron-variant | CHAF1B | GRCh38.p7 | 21:36407317 | AAAAAAAAAAAAAAA[A/T]GTATATGTTCAAGGA | 8208 |
| rs568468793 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-5-prime, upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36380176 | GGCGTGAGCCATCAC[A/G]CCCAGCTGGCTGTAT | 8208 |
| rs568596512 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CHAF1B | GRCh38.p7 | 21:36387320 | CCCGACCCGGGGCTC[A/G]AGTGATCCTCCCTCT | 8208 |
| rs568631757 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | CHAF1B | GRCh38.p7 | 21:36395998 | GTTCTGTCTTGTTTT[G/T]TGTGGTTTTTTTTTT | 8208 |
| rs568711627 | snp | A/T | | | utr-variant-3-prime | MORC3 | GRCh38.p7 | 21:36376499 | TGGAAAGAGCAAATA[A/T]ATGAAGATTGTTTTT | 8208 |
| rs568860365 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36403248 | GGATCACTTGAGGTC[A/G]AGAGTTCATGACCAG | 8208 |
| rs568896091 | snp | A/C/G | 4.94477e-05 | 0.0049721 | intron-variant | CHAF1B | GRCh38.p7 | 21:36391677 | CTCTGCGGTAACTTG[A/C/G]GAGGGACCATGGCAG | 8208 |
| rs568896556 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36411302 | TATTTTTGATAGAGA[C/T]GGGGTTTTGCCATGT | 8208 |
| rs568898753 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | CHAF1B | GRCh38.p7 | 21:36410465 | TTGATACTACTTACT[-/A]TTTTTTGTTTTTTTC | 8208 |
| rs568913743 | in-del | -/TTTTTT | | | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36379899 | TTTTTTTTTTTTTTT[-/TTTTTT]GAGACAAAGTATCAT | 8208 |
| rs568963219 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CHAF1B | GRCh38.p7 | 21:36383824 | CGACTAATTTTTTGT[A/G]ATTTTTGTAGAGATG | 8208 |
| rs569058128 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36391183 | TTAAGGTGATTTTGT[A/G]TAGCTCTGATCTGTT | 8208 |
| rs569103378 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36407720 | CAGTGACTCACGCCT[G/T]TAATCCCAGCACTTT | 8208 |
| rs569116913 | snp | C/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36386333 | TTCTTTTACTTAAAA[C/G]CAGTGTCGGCTGGGC | 8208 |
| rs569223539 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | CHAF1B | GRCh38.p7 | 21:36416487 | TGTAAATGGATTTCT[A/G]TAACAGAAGTGACAT | 8208 |
| rs569236661 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36389824 | ACGCTGATTTGTAGA[A/G]GGAAAAGTGGGGAGC | 8208 |
| rs569287285 | snp | C/T | 1.64741e-05 | 0.00286998 | stop-gained | CHAF1B | GRCh38.p7 | 21:36399543 | CGAGTATACAGTATA[C/T]AGAAGAAGCGTGTGG | 8208 |
| rs569291155 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | MORC3 | GRCh38.p7 | 21:36376891 | GAGGCCGAGGCGGGC[A/G]GATCACCTGAGGTCG | 8208 |
| rs569342981 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36416043 | ACAGGCGTGAGCCAC[C/T]GCGCCCAGCTTGCCC | 8208 |
| rs569699689 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36406371 | GCTCACTGCAACCTC[C/T]ATCTCCTGAGTTCAA | 8208 |
| rs569921621 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36387131 | AAGAAGGCGGAGGGG[C/G]ACAGTAGACATTTAT | 8208 |
| rs569959486 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36405007 | CCTTGGCCTCCCAAA[A/G]TGTTGGGATTACAGG | 8208 |
| rs569975842 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36392715 | CGGGCAGAGACGCTC[C/T]TCACCTCCCAGACAG | 8208 |
| rs570082918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36392473 | GGCGGCCGGGTAGAG[A/G]GGCTCCTCACTTCCC | 8208 |
| rs570126146 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36399077 | AATCTCGCTCTGTTG[C/T]CCAGGCTGGAGTGCA | 8208 |
| rs570218407 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHAF1B | GRCh38.p7 | 21:36412422 | TGGAGTGCAGTGGAA[C/T]GATCGTGGCTCACTA | 8208 |
| rs570312209 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | CHAF1B | GRCh38.p7 | 21:36401988 | TCAAGTGATCCGCCC[A/C/G]CCTTGGCCTCCCAAA | 8208 |
| rs570530162 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36410213 | GGTGATCCACCCACC[C/T]TGGCCTCCCAAAGTA | 8208 |
| rs570601385 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CHAF1B | GRCh38.p7 | 21:36395430 | ACAGGATAGGGGTTA[A/G]TCCCATATGCTATGG | 8208 |
| rs570689788 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36409750 | TGATCCACCTGCCTC[A/G]GCCTCCCAAAATGCT | 8208 |
| rs570956905 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36380941 | TACTCCAGGGTATTT[C/G]AGATGTAAGGTATTT | 8208 |
| rs570966931 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CHAF1B | GRCh38.p7 | 21:36409110 | TCCGCTTGCCTCGGC[C/T]TCCCAAAGTGCTGGG | 8208 |
| rs570980628 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CHAF1B | GRCh38.p7 | 21:36388205 | ACTGTTCTAGGGAAT[A/G]TGGTAGAGTCAGGGA | 8208 |
| rs570994087 | snp | A/T | 0.000820906 | 0.020243 | intron-variant, upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36380323 | ACTGAATTAAGGTAA[A/T]TTGAGTATAGAATTT | 8208 |
| rs571049267 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CHAF1B | GRCh38.p7 | 21:36393554 | CCTCCTGGGTTCAAG[C/T]GATTCTCCTACCTCA | 8208 |
| rs571060935 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CHAF1B | GRCh38.p7 | 21:36395083 | TTGGAGACGGAGTTT[C/T]GCTCTTGTCCAGGTT | 8208 |
| rs571125146 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CHAF1B | GRCh38.p7 | 21:36392277 | CATCCCAAGGCAGAA[G/T]AATTTTTCTTAGTAC | 8208 |
| rs571143407 | in-del | -/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | MORC3 | GRCh38.p7 | 21:36375541 | TTTTGAATGTAAATA[-/T]TTTGTAATTAAGCCT | 8208 |
| rs571213479 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CHAF1B | GRCh38.p7 | 21:36412442 | GTGGCTCACTACAAC[C/G]TCCGCCTCCTGGGTT | 8208 |
| rs571231935 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36378575 | GGTGGGCTCCTGTAA[G/T]CCCAGCTACTTGGGA | 8208 |
| rs571298466 | snp | A/C | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36414487 | GAAGGTATTCCTTGA[A/C]CTATTTTTGGTATTA | 8208 |
| rs571376081 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CHAF1B | GRCh38.p7 | 21:36403325 | TAATGATGTGGTGGC[A/G]CATACCCTGTAATCC | 8208 |
| rs571441408 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CHAF1B | GRCh38.p7 | 21:36383906 | GCCCACCTCGGCCTC[C/T]TAAAGTGCTGGGATT | 8208 |
| rs571445726 | in-del | -/TGAGT | 0.00953873 | 0.0683987 | upstream-variant-2KB, intron-variant | CHAF1B | GRCh38.p7 | 21:36383468 | GTTTTTTTTCGAAGC[-/TGAGT]TAAGAGTTAGTCCCT | 8208 |
| rs571469049 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36406652 | GATGTTTTGAAGTAT[A/G]TATATGTTGTGGAAT | 8208 |
| rs571520010 | snp | C/T | 0.00597247 | 0.0543191 | downstream-variant-500B | MORC3 | GRCh38.p7 | 21:36376813 | AGAGCATGTATATTC[C/T]GTTTTCAAAAGCTTT | 8208 |
| rs571719858 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36411365 | GTGATCCACCCGGCT[C/T]GGCCTCCCAAAGTGC | 8208 |
| rs571727084 | snp | A/G | 0.000399281 | 0.0141238 | missense, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36387676 | CGTCATACCAAAGCC[A/G]TCAATGTTGTGCGTT | 8208 |
| rs571727351 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36394155 | GATCTTGGCTCACTG[A/C]AATCTCTGCCTCCCA | 8208 |
| rs571769639 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | CHAF1B | GRCh38.p7 | 21:36417174 | CCTCCTGGGCTCGAG[C/T]GATCCTTCCACCTCA | 8208 |
| rs571775128 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | CHAF1B | GRCh38.p7 | 21:36416049 | GTGAGCCACCGCGCC[C/T]AGCTTGCCCATGACA | 8208 |
| rs571791597 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36381442 | TTGGGCATTTCTAGG[C/T]CTTTTTAGTAGACTG | 8208 |
| rs571846339 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CHAF1B | GRCh38.p7 | 21:36383228 | CTAGTATCCCGAGTA[A/G]CTGGGATTACAGGCA | 8208 |
| rs571857716 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | CHAF1B | GRCh38.p7 | 21:36416581 | ACATGAACGTTTTAA[C/T]GTAGTAAATCCTCTT | 8208 |
| rs571942061 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36382578 | TGAGTCTGTTTCTGT[C/T]GCCCAGACTGGAGTG | 8208 |
| rs572217911 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36406636 | TAGTTGTGTATGACA[C/T]GATGTTTTGAAGTAT | 8208 |
| rs572340632 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36413715 | TGGACACCTCTTCCT[C/G]TTGGTGATGCCAGGA | 8208 |
| rs572399706 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36412684 | GTGAAAATTGCTAGT[A/G]GCACAGATAGGTTGC | 8208 |
| rs572405526 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36378431 | CTGGGCGCAGTGGCT[C/T]GTGCCTGTAATCCCA | 8208 |
| rs572461299 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36386504 | AGCTACTTGGGAAGT[A/T]GAAGTGAGAGGATCG | 8208 |
| rs572492961 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | CHAF1B | GRCh38.p7 | 21:36385329 | GGGCGGGACCTGAGG[A/G]CCGCTGGAGGGGCGG | 8208 |
| rs572544827 | in-del | -/C | 0.119473 | 0.21322 | intron-variant | CHAF1B | GRCh38.p7 | 21:36392512 | GGCCGGGCAGAGGCG[-/C]CCCCCCACCTCCCGG | 8208 |
| rs572657347 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHAF1B | GRCh38.p7 | 21:36392502 | CCAGACAGGGCGGCC[A/G]GGCAGAGGCGCCCCC | 8208 |
| rs572702759 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36405471 | TCACTCTGTCACCCA[G/T]GCTGGAGTACAGTGG | 8208 |
| rs572744207 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CHAF1B | GRCh38.p7 | 21:36398429 | CAGTGGTGCGATCTC[G/T]GCATACTGTAACCTC | 8208 |
| rs572782745 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36397873 | GCTGGGATTACAGGC[A/G]CATGCCACCATGCCC | 8208 |
| rs572845693 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36382765 | AGGCTGGAGTGCAAT[A/G]GCGCAATCTCGGCTC | 8208 |
| rs572870800 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36416190 | AGCTCAGTTCCGTGT[C/T]TTGGCTCTGTATTCT | 8208 |
| rs572891145 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36411876 | TGGGATTACAGGTGC[A/C/G]CACCACTACGCCTGG | 8208 |
| rs572907823 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHAF1B | GRCh38.p7 | 21:36415815 | TGGAATGCAGTGGCA[C/T]GATTTCGGCTCACTG | 8208 |
| rs573007469 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36415014 | CAGCAGAGTGTTCAC[A/G]AGACCGTCGGTAATG | 8208 |
| rs573095224 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36414467 | CTGTTTGTTTTTATG[C/T]GACGGAAGGTATTCC | 8208 |
| rs573140284 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36386622 | GAATGAATGAATTAA[C/T]GTATGTCAACAAACT | 8208 |
| rs573174799 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | CHAF1B | GRCh38.p7 | 21:36400990 | ATAGTAATGCTTCCC[A/G]GGTGCGGTGGCTCAG | 8208 |
| rs573231290 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36388367 | TTCTGGTTTTGTTGG[A/C]TTGTTAGTTTAACAT | 8208 |
| rs573256775 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36409150 | ATGAGTCATTGCACC[C/T]GGCTTGTATTTTTTT | 8208 |
| rs573282867 | in-del | -/A | 0.0578636 | 0.159949 | intron-variant | CHAF1B | GRCh38.p7 | 21:36396654 | ACCACACCCTGTCTC[-/A]AAAAAAAAAGAAAAA | 8208 |
| rs573355386 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36389901 | CACATGGCAGCCCCC[A/G]TTTTCCAAAGTCCCT | 8208 |
| rs573413046 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CHAF1B | GRCh38.p7 | 21:36412494 | CCTCCCGAATAGCTG[A/G]GATTACAGGCGCCCA | 8208 |
| rs573487728 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36379682 | GAAGAAAGTCTGGTT[A/G]AGAGTTAACAAGAAA | 8208 |
| rs573498508 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36411978 | AACGATCCTCCTGCC[C/T]CAGCCTCCCAAAGTG | 8208 |
| rs573541772 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36398567 | GTTTCACCGTATTGA[C/T]GATGCTGGTCTCAAA | 8208 |
| rs573628065 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | CHAF1B | GRCh38.p7 | 21:36383996 | TTTGAGGTTTTGAAC[A/G]AATACTTTTTTTTTT | 8208 |
| rs573630489 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36405596 | CACCATGCCTGGCTA[A/G]TTTTCTTATTTTTTT | 8208 |
| rs573690264 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36404504 | CAATGGCACGATCTC[A/G]GCTCACAGCAACCTC | 8208 |
| rs573714241 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CHAF1B | GRCh38.p7 | 21:36383690 | GTCTCGCTCTCTCGC[A/C]CAGGCTGGAGTGCAG | 8208 |
| rs573716253 | in-del | -/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36399037 | ATGTGACTTACCAAT[-/T]TTTTTTTTTTTTTTT | 8208 |
| rs573978224 | snp | C/T | | | utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36382149 | AGTAATGTTGACCAC[C/T]TATCGGGTATGTCTT | 8208 |
| rs574096662 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36397163 | CAGCTCCCCTCCCCC[A/G]GTCCACATGTGTGAT | 8208 |
| rs574105183 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36405156 | TTCTTTGTGGTGTTA[A/G]TAAGTGTGGGAAAAA | 8208 |
| rs574108341 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36380594 | TAAATATATATATAT[A/T]TTTTGAGACAGGCTC | 8208 |
| rs574249440 | snp | C/T | 0.000296594 | 0.0121741 | intron-variant | CHAF1B | GRCh38.p7 | 21:36402872 | TTTCGTAGCTTTGGA[C/T]TTAAAGGAATGATGG | 8208 |
| rs574348813 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CHAF1B | GRCh38.p7 | 21:36392479 | CGGGTAGAGGGGCTC[C/T]TCACTTCCCAGACAG | 8208 |
| rs574358144 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36411400 | ATTCTAGGCGTGAGC[C/G]ATTGCACCTGGTCAG | 8208 |
| rs574553134 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | CHAF1B | GRCh38.p7 | 21:36398357 | TGATTTTTATTTTTA[-/T]TTTTTTTTAAATTGT | 8208 |
| rs574561388 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36400460 | TGGGTGACAAGAGCG[A/G]AACTCAGTCTCAAAA | 8208 |
| rs574599471 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36415721 | GTTTAACAGCATCCC[C/T]GGCTGCTACTTCTTG | 8208 |
| rs574619058 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36399869 | TGCACGGTGGAATCA[A/C]CTGGGAAGAATTACA | 8208 |
| rs574805448 | in-del | -/GGA | 0.000301942 | 0.0122833 | cds-indel | CHAF1B | GRCh38.p7 | 21:36413214 | CTTGCCGGGGCCTTC[-/GGA]GGAGAAGACCCTGCA | 8208 |
| rs574883556 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36413783 | TTGCAGTCTTTGTGG[C/T]CCTTCAGCCTTTCCC | 8208 |
| rs575102096 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36386598 | GCCAGACCCTTCTCT[C/T]AAGTAAATGAATGAA | 8208 |
| rs575126162 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CHAF1B | GRCh38.p7 | 21:36399207 | GCCCGGCTAATTTTT[G/T]GTATTTTTGGTAGAG | 8208 |
| rs575162443 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | CHAF1B | GRCh38.p7 | 21:36416714 | ACTCCTTTTCAATAA[A/G]AATTAGGAAGATGAG | 8208 |
| rs575301402 | snp | A/G | 0.000839789 | 0.0204741 | synonymous-codon | CHAF1B | GRCh38.p7 | 21:36411512 | GTTTGCTGTGGCCTC[A/G]GAGGATTCCGTGCTT | 8208 |
| rs575327774 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CHAF1B | GRCh38.p7 | 21:36390655 | CCTGTGAGGTAGATA[C/T]ATTGTTATCCTCATT | 8208 |
| rs575398353 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B | MORC3 | GRCh38.p7 | 21:36376972 | AATACAAAATTAGCC[A/G]GGTGTGGTGATGCAT | 8208 |
| rs575422916 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime, intron-variant | CHAF1B | GRCh38.p7 | 21:36384726 | GTGTGTTTCTTTTAT[C/T]CAGTAAAAGCAGCGC | 8208 |
| rs575437761 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | MORC3 | GRCh38.p7 | 21:36375968 | TTTAACAGAAAAAAG[A/G]TATTGAAATATTAAA | 8208 |
| rs575497995 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36396410 | CAGGCACAGTGGCTC[A/G]GGCCTGTAATCCCAG | 8208 |
| rs575560254 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36381142 | TTTTTTTTCTTTTGC[A/G]ACAGGTCTTGCTCTG | 8208 |
| rs575570736 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36395889 | GTTGTTGGCTGCCAC[C/T]GCAGCACTGTGTCAG | 8208 |
| rs575577429 | snp | C/T | | | intron-variant, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36381817 | AGTCCCATGATCTGC[C/T]GTCTGCAAGATGGAG | 8208 |
| rs575600933 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36394116 | GGAGTCTCACTCTGT[C/T]GCCAGGCTGGAGTGT | 8208 |
| rs575712012 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36398462 | CCTCCTAGGTTCAAG[C/T]GATTCTCCTGCCTCA | 8208 |
| rs575734721 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | CHAF1B | GRCh38.p7 | 21:36406533 | TCAGGTGATCCACCC[G/T]CCTCAGCCTCCCAAA | 8208 |
| rs575739511 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36415599 | GGTGAGCCAGGGAGT[A/G]GGTTCAGCAGGAGAT | 8208 |
| rs575798407 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36403094 | TTTTAAGAAGATTTC[C/T]AAGTGATTGTAATGT | 8208 |
| rs575925562 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36392905 | AGACCACGCCAGTGC[C/T]CTCCAGCCTGGGCAA | 8208 |
| rs575967875 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36378396 | TACTTACTTACTTTT[C/T]GTTAGAAAGAATATA | 8208 |
| rs576052748 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 21:36377659 | AAAATCAGTGAAAGC[C/T]GAGTGAGCACACAGA | 8208 |
| rs576089552 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36384241 | ATTTGTGAATGAACA[A/G]CATTTATGAGAAATT | 8208 |
| rs576173828 | snp | C/T | 1.68366e-05 | 0.00290138 | missense | CHAF1B | GRCh38.p7 | 21:36413234 | AGAAGACCCTGCAGC[C/T]CAGTAGTCAAAACAC | 8208 |
| rs576187817 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36412561 | GAGACAGGGTTTCAC[C/T]ATGTTGGCCAGGCTG | 8208 |
| rs576380057 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36401254 | CCTGGGCAACAAGAG[C/T]GAAACTCTGGCTCAA | 8208 |
| rs576498920 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36392022 | AGGGAAGGTCAGCAG[A/G]TAAACAAGTGAACAA | 8208 |
| rs576508323 | snp | C/G | | | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36379927 | AGTATCATTCTGTTG[C/G]CCAGGCTGGAGTGCA | 8208 |
| rs576535275 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36397758 | ACACAGTCTCACTCT[A/G]TCACCCAGGCAGGTG | 8208 |
| rs576716769 | snp | C/G | 0.000136156 | 0.00824982 | intron-variant | CHAF1B | GRCh38.p7 | 21:36415269 | AATGAGCCATCACCC[C/G]TCTACTTTTTTTTTT | 8208 |
| rs576776223 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36404219 | GATTCTCCTGCCTCA[G/T]CCTCCTGAGTAGCTG | 8208 |
| rs576786147 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36381990 | GAAGAGACAGAATTT[A/G]CCCTTCCTCTACTTT | 8208 |
| rs576810369 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36403503 | TACTATTTAAACCCT[G/T]TCAATGAATGCTTTT | 8208 |
| rs576907340 | snp | C/T | 0.0130921 | 0.0798413 | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36379375 | TCTTAAGCTCCTGGA[C/T]TCAAGCAGTCCACCC | 8208 |
| rs577044518 | snp | A/C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36412484 | CCTGCCTCAGCCTCC[A/C/T]GAATAGCTGGGATTA | 8208 |
| rs577091448 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CHAF1B | GRCh38.p7 | 21:36394770 | AGGATCTCACTCTGC[C/T]GCCCAGGCTGGAGTG | 8208 |
| rs577177011 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36394258 | ATTTTTTGTATTTTA[A/G]TAGAGACGTGGTTTC | 8208 |
| rs577198914 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHAF1B | GRCh38.p7 | 21:36414451 | GTATTTTACAATTTT[C/T]CTGTTTGTTTTTATG | 8208 |
| rs577213737 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHAF1B | GRCh38.p7 | 21:36400509 | TAAAATAAAAATAAA[A/G]ATATGGATGCCTTGG | 8208 |
| rs577284173 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHAF1B | GRCh38.p7 | 21:36413861 | TCCCCTGCTGGTTGT[A/G]AGCCCCCAAGGACAG | 8208 |
| rs577338977 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36407839 | AAAAATTAGCCGGGC[A/G]TCGTGGCAGGTGCCT | 8208 |
| rs577636392 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36411950 | GCCAGGCTGGTATCA[A/T]ACTCCTGGGCTCAAC | 8208 |
| rs577637670 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36403649 | ACTTGTGGAAGCAGC[A/C]GTGGTCAAAATCAAA | 8208 |
| rs577642104 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | CHAF1B | GRCh38.p7 | 21:36392452 | GGTACACCTCCCAGA[C/T]GGGGTGGCGGCCGGG | 8208 |
| rs577683885 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36396478 | CCAGCATGGGCAACA[C/T]GGCAAAACCCTCTCT | 8208 |
| rs577719192 | snp | C/T | 0.000280027 | 0.0118294 | synonymous-codon | CHAF1B | GRCh38.p7 | 21:36402826 | ACTGAGTTTCACTCC[C/T]GACGGATCTTTGCTT | 8208 |
| rs577721064 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CHAF1B | GRCh38.p7 | 21:36396004 | TCTTGTTTTGTGTGG[G/T]TTTTTTTTTTATTTT | 8208 |
| rs577747343 | snp | C/T | | | upstream-variant-2KB, intron-variant | CHAF1B | GRCh38.p7 | 21:36384086 | TGTTGGCTCATCAAG[C/T]TGGCACTGAAGTCGG | 8208 |
| rs577772174 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36406003 | TTTGCCTCACCACAT[A/G]TCAGAAGATCCTATA | 8208 |
| rs577805004 | snp | A/T | | | upstream-variant-2KB, intron-variant | CHAF1B | GRCh38.p7 | 21:36383827 | CTAATTTTTTGTAAT[A/T]TTTGTAGAGATGGGG | 8208 |
| rs577819161 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CHAF1B | GRCh38.p7 | 21:36383632 | GTTAGAATTGCGTTA[C/T]AGGAATTCCCTTTTT | 8208 |
| rs577834157 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CHAF1B | GRCh38.p7 | 21:36408344 | GGAAAGGCGAGTCTC[A/G]GCCTTTGGATGGCAT | 8208 |
| rs577845523 | snp | C/T | 0.000150636 | 0.0086773 | | | GRCh38.p7 | 21:36377440 | CAAGATATGAGACTT[C/T]GAAAATGTGGCTCAC | 8208 |
| rs577892886 | in-del | -/TTAC | | | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36378376 | ATATGCTCCTAATGG[-/TTAC]TTACTTACTTACTTT | 8208 |
| rs577933316 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B | MORC3 | GRCh38.p7 | 21:36377059 | GGTGGAGGTTGCAGC[G/T]AGCCGAGATCACACC | 8208 |
| rs577966663 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | MORC3 | GRCh38.p7 | 21:36376414 | TTGAACATTCAATCC[A/G]TTCATTTTGTATGTA | 8208 |
| rs578021032 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36400779 | GAAGGATTTTGACTT[C/T]CAAATAATTGGCAAA | 8208 |
| rs578208954 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36415705 | CTGTGTATTATGCGA[C/T]GTTTAACAGCATCCC | 8208 |
| rs745400946 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36382200 | TAAAATTAACTATCA[C/T]AGTATTTCTTTTGGA | 8208 |
| rs745421124 | in-del | -/T | 0.422426 | 0.188603 | intron-variant | CHAF1B | GRCh38.p7 | 21:36415748 | TTGCCCATGACATTC[-/T]TTTTTTTTTTTTTCT | 8208 |
| rs745438796 | snp | A/G | 1.64874e-05 | 0.00287113 | synonymous-codon | CHAF1B | GRCh38.p7 | 21:36413052 | ACATCGAGGGTCTTC[A/G]CCAGGACCCAGACCG | 8208 |
| rs745452989 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36386746 | TGAGACGGAGTCTTG[C/T]TCTGTTGCCCAGGTG | 8208 |
| rs745473711 | snp | G/T | 1.64789e-05 | 0.0028704 | missense | CHAF1B | GRCh38.p7 | 21:36399522 | TGTTCTTTCTTCAGG[G/T]TGCTGCGAGTATACA | 8208 |
| rs745521824 | in-del | -/A | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36389604 | GTGAGAGTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 8208 |
| rs745523995 | snp | C/T | 4.98633e-05 | 0.00499291 | missense | CHAF1B | GRCh38.p7 | 21:36413117 | CCAGCAGCCCCGGCA[C/T]GACTCCCCCTCAGGC | 8208 |
| rs745524676 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36395317 | CCTCCCAAAGTGCTG[A/G]GATTACAGGCATGAG | 8208 |
| rs745535693 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36409787 | ACAGGTGTGAGCCCC[C/T]GTGCCCGGCCTGGTT | 8208 |
| rs745546614 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36412024 | TGAGCCACCACGCCC[A/G]GCCCCAATTTTGTTT | 8208 |
| rs745577741 | in-del | -/ATC | | | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36378320 | ACTAAACATTTCCAT[-/ATC]ATTCTTTCAAAAAGC | 8208 |
| rs745721379 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36404944 | AGATGGGGTTTCGCC[A/G]TGTTGGCCAGGCTGG | 8208 |
| rs745732322 | snp | C/T | 1.64743e-05 | 0.00287 | synonymous-codon | CHAF1B | GRCh38.p7 | 21:36399596 | GTCTGGAATAGGGGC[C/T]GAAGGAGAGGTATAA | 8208 |
| rs745779016 | snp | A/G | 1.87184e-05 | 0.00305922 | utr-variant-3-prime | CHAF1B | GRCh38.p7 | 21:36416368 | GTCTGGACCCTTGAT[A/G]GGACCTCGGCTTCTG | 8208 |
| rs745794653 | snp | A/C | 1.65754e-05 | 0.00287879 | intron-variant | CHAF1B | GRCh38.p7 | 21:36409515 | CTCTCCGAAACAGGT[A/C]ACCAGAGTGGGGTGG | 8208 |
| rs745806625 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36415702 | GTCCTGTGTATTATG[C/T]GATGTTTAACAGCAT | 8208 |
| rs745833922 | snp | C/G | 0.000273598 | 0.0116929 | utr-variant-5-prime, upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36380303 | GTACTGTGATCTGAA[C/G]CATGACTGAATTAAG | 8208 |
| rs745930940 | snp | C/T | | | missense | CHAF1B | GRCh38.p7 | 21:36411598 | ACACCCTCAGTGACA[C/T]TTCATGGTGAGTGGC | 8208 |
| rs745934263 | snp | C/T | | | | | GRCh38.p7 | 21:36377622 | AAACAGTCCACAGTC[C/T]TCAAACAGGACCTAG | 8208 |
| rs745977331 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36411389 | AAAGTGCTGGGATTC[C/T]AGGCGTGAGCCATTG | 8208 |
| rs746002182 | snp | C/T | 1.64735e-05 | 0.00286993 | missense | CHAF1B | GRCh38.p7 | 21:36411511 | TGTTTGCTGTGGCCT[C/T]GGAGGATTCCGTGCT | 8208 |
| rs746025510 | snp | C/T | 4.94964e-05 | 0.00497451 | missense, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36391593 | ATGATAACAAGGAGC[C/T]GGAGCAGATCGCTTT | 8208 |
| rs746272314 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36388046 | CAGGCTGATCTCGAA[C/T]TCCTGACCTCAGGTG | 8208 |
| rs746327888 | snp | A/G | 6.59435e-05 | 0.00574172 | intron-variant | CHAF1B | GRCh38.p7 | 21:36402890 | AAAGGAATGATGGCC[A/G]AGTGGGGATGTCTGC | 8208 |
| rs746343577 | in-del | -/C | 1.65644e-05 | 0.00287783 | intron-variant | CHAF1B | GRCh38.p7 | 21:36408725 | TTGCTGAAACAGTGA[-/C]TTTTCTTTCCTCTCC | 8208 |
| rs746380922 | snp | A/G | 1.64768e-05 | 0.00287021 | missense | CHAF1B | GRCh38.p7 | 21:36402788 | ATGTTTCACGACGAC[A/G]GCATGAAGTCTTTCT | 8208 |
| rs746391127 | in-del | -/TTTT | | | intron-variant, upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36381114 | TTCTTCTTCTTCTTT[-/TTTT]TTTTTTTTTTTTTTT | 8208 |
| rs746473282 | in-del | -/A | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36402721 | GTGTAGAAAACAAAC[-/A]AAAAAAAATAATAAA | 8208 |
| rs746524368 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36408159 | AGAGCAGCAGTGTAT[A/G]ATGGTCACTCTGACA | 8208 |
| rs746535919 | in-del | -/T | 4.94401e-05 | 0.00497168 | intron-variant | CHAF1B | GRCh38.p7 | 21:36387780 | CCAGATAGATACCTG[-/T]TGTGTCTTGTGTCAG | 8208 |
| rs746615188 | snp | C/T | 0.000137014 | 0.00827578 | intron-variant, upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36380342 | AGTATAGAATTTTTT[C/T]TGTTCTAGGCAATTG | 8208 |
| rs746654188 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36407114 | CAAGACCAGCCTGGC[C/T]AACATGGCAAAACCC | 8208 |
| rs746682092 | snp | A/G | 1.64792e-05 | 0.00287042 | intron-variant | CHAF1B | GRCh38.p7 | 21:36399610 | CTGAAGGAGAGGTAT[A/G]AAATATTTTGCCATT | 8208 |
| rs746723654 | snp | C/T | 4.03918e-05 | 0.0044938 | utr-variant-3-prime | CHAF1B | GRCh38.p7 | 21:36416386 | ACCTCGGCTTCTGCT[C/T]GAAGCCTACCAGGCT | 8208 |
| rs746741184 | in-del | -/TGTG | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36389760 | GAGTGCATGAAGGGA[-/TGTG]TGTGTGTGTGTGTGT | 8208 |
| rs746796755 | snp | A/C | | | intron-variant, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36381789 | GTGGCTTAAGTGGTT[A/C]TGGAGTCTGAGAAGT | 8208 |
| rs746908856 | in-del | -/AC | | | downstream-variant-500B | CHAF1B | GRCh38.p7 | 21:36417296 | CATATATATATATAT[-/AC]ACACACACACAAGTA | 8208 |
| rs746922629 | snp | C/T | 3.29826e-05 | 0.00406082 | intron-variant | CHAF1B | GRCh38.p7 | 21:36391706 | AGTGATCTCTGTTTA[C/T]GATGAGTGCATTAAA | 8208 |
| rs747075155 | snp | A/G | | | utr-variant-3-prime | MORC3 | GRCh38.p7 | 21:36375605 | GTGTTTTTCACCAAG[A/G]GCTTTTCAGGTTGCC | 8208 |
| rs747178588 | snp | A/T | | | synonymous-codon | MORC3 | GRCh38.p7 | 21:36375242 | CGATGTTGATGTAGT[A/T]GATGAGATTTTAGGA | 8208 |
| rs747178648 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36402497 | ACACATATATACATA[C/T]AGCTTTACCTAACAA | 8208 |
| rs747201200 | snp | A/T | 6.63119e-05 | 0.00575774 | synonymous-codon | CHAF1B | GRCh38.p7 | 21:36415328 | CTTAAAGACGGACAC[A/T]CCACCAAGTTCTGTA | 8208 |
| rs747214087 | snp | A/C | 1.65638e-05 | 0.00287778 | missense | MORC3 | GRCh38.p7 | 21:36375210 | GTGCCTGATCTTGAT[A/C]TTCAGCAAGTGAATT | 8208 |
| rs747226536 | snp | A/G | 5.58852e-05 | 0.00528578 | intron-variant | CHAF1B | GRCh38.p7 | 21:36413339 | TTGTTGGAACAAGAT[A/G]TCATTGCAAAATGAA | 8208 |
| rs747255684 | snp | G/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36402597 | TTCAGTTTCATTTAT[G/T]ATTATGTCAACAATA | 8208 |
| rs747380139 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36398476 | GCGATTCTCCTGCCT[C/T]ATCCTCCTGAGTAGC | 8208 |
| rs747426782 | snp | A/G | 1.64738e-05 | 0.00286995 | synonymous-codon, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36387720 | GGAAATTTTAGCATC[A/G]GGAGGAGATGGTGAG | 8208 |
| rs747466664 | snp | A/C | 1.66205e-05 | 0.00288271 | intron-variant | CHAF1B | GRCh38.p7 | 21:36408713 | TTGGTGAACAGTTTG[A/C]TGAAACAGTGACTTT | 8208 |
| rs747477986 | snp | G/T | 1.67699e-05 | 0.00289563 | intron-variant | CHAF1B | GRCh38.p7 | 21:36408865 | TTTGAAATGTTTACA[G/T]TTTTTTTAGACGGAG | 8208 |
| rs747525628 | snp | G/T | 1.65343e-05 | 0.00287521 | intron-variant | CHAF1B | GRCh38.p7 | 21:36387562 | ATAATATGTGCCCAT[G/T]CTATGTTTTTCAAAT | 8208 |
| rs747566889 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36411315 | GACGGGGTTTTGCCA[C/T]GTTGCTTAGGCAGGT | 8208 |
| rs747697878 | snp | A/C | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36406973 | CTTGTAAGGAAATAT[A/C]GGAGGACATTCTAGG | 8208 |
| rs747714663 | snp | G/T | 1.66338e-05 | 0.00288386 | intron-variant | CHAF1B | GRCh38.p7 | 21:36386291 | GAGATAGACATCCGG[G/T]AACACTGCTTGAAGC | 8208 |
| rs747758462 | snp | C/T | 1.64838e-05 | 0.00287083 | missense | CHAF1B | GRCh38.p7 | 21:36402774 | CAAGAAGCTACCGGA[C/T]GTTTCACGACGACAG | 8208 |
| rs747848592 | snp | A/C/G | 3.30138e-05 | 0.00406276 | missense, synonymous-codon, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36386229 | TGGGAGGATCCACAG[A/C/G]CTGGCGTCTGCCGGC | 8208 |
| rs747871705 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36394916 | TTTGTATTTTTAGTA[A/G]AGACGGGTTTCATCA | 8208 |
| rs747890403 | snp | A/G | | | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36378680 | GACTGGTGACAGAGC[A/G]AGACTCCGTCTCAAA | 8208 |
| rs747978369 | in-del | -/AAAC | 0.000117537 | 0.00766517 | intron-variant | CHAF1B | GRCh38.p7 | 21:36402714 | AGCTTTGTGTGTAGA[-/AAAC]AAACAAAAAAAATAA | 8208 |
| rs748061562 | in-del | -/T | | | downstream-variant-500B | MORC3 | GRCh38.p7 | 21:36377129 | TCAAAAAAAAAGGAC[-/T]TTTCTTTGTATAAAT | 8208 |
| rs748104009 | snp | C/T | 0.0021845 | 0.0329769 | missense, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36394606 | GGAATTTAATGGCTT[C/T]TGCCTCTGTGGATAA | 8208 |
| rs748107004 | snp | G/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36393941 | GTCTCACTCTGTTGC[G/T]CAGGCTGGAGTGCAG | 8208 |
| rs748125049 | snp | A/G | 1.64762e-05 | 0.00287016 | missense | CHAF1B | GRCh38.p7 | 21:36413018 | CTCCTGATACAGCAA[A/G]GAAAACCAAGAGTCA | 8208 |
| rs748130447 | snp | G/T | | | splice-acceptor-variant, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36382018 | TTTTTGTTCTTTTCA[G/T]ACTCAACAGGTTGGA | 8208 |
| rs748226258 | snp | A/C | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36389088 | CCCAGCTTGGCAGCT[A/C]CTCTGGTTTGACATC | 8208 |
| rs748277584 | snp | A/G | 1.65644e-05 | 0.00287783 | missense | MORC3 | GRCh38.p7 | 21:36375240 | TACGATGTTGATGTA[A/G]TTGATGAGATTTTAG | 8208 |
| rs748301544 | in-del | -/TTTTTTTTTTT | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36397720 | TGTACTTAGTAAATC[-/TTTTTTTTTTT]TTTTTTTTTTAGACA | 8208 |
| rs748341082 | snp | G/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36413766 | CAATGTACCCTCTCT[G/T]TTTGCAGTCTTTGTG | 8208 |
| rs748397459 | snp | A/T | 1.65891e-05 | 0.00287998 | intron-variant | CHAF1B | GRCh38.p7 | 21:36415420 | ACTGGTTTAATATAA[A/T]GAAAGGTAGAGTATC | 8208 |
| rs748398428 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36414737 | CTACCTCAGCCTCTC[A/G]GGTAGCTGGGATTAC | 8208 |
| rs748419275 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36399889 | GAAGAATTACAAATA[C/T]GGGTGCTGGCCGGGC | 8208 |
| rs748425761 | in-del | -/GAGGGA | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36393233 | GAGAGGGAGACGGTG[-/GAGGGA]GAGGGAGAGGGAGAG | 8208 |
| rs748529965 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36414830 | GTTGGTCAAGCTGGT[C/T]GAAAACTCCTGACCT | 8208 |
| rs748618760 | snp | C/T | 3.30819e-05 | 0.00406692 | intron-variant | CHAF1B | GRCh38.p7 | 21:36391545 | TGTTACTGAATCACC[C/T]TGCAGATGCTGTCAT | 8208 |
| rs748789062 | in-del | -/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36393447 | AAGATACAGCTATCC[-/T]TTTTTTTTTTTTTTT | 8208 |
| rs748844043 | snp | G/T | 1.66946e-05 | 0.00288912 | intron-variant | CHAF1B | GRCh38.p7 | 21:36386302 | CCGGGAACACTGCTT[G/T]AAGCAATAGTTTTCA | 8208 |
| rs748914337 | snp | C/T | 4.94425e-05 | 0.0049718 | missense | CHAF1B | GRCh38.p7 | 21:36413038 | ACCAAGAGTCAGACA[C/T]ATCGAGGGTCTTCGC | 8208 |
| rs748939455 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36382395 | AGTCATAGGGTAGGC[A/G]TATCATTAACTTTAT | 8208 |
| rs748965823 | snp | A/G | 3.59305e-05 | 0.00423839 | intron-variant | CHAF1B | GRCh38.p7 | 21:36412856 | GTGTTGGTAAGGTCT[A/G]TAACTTTTCCCTGTT | 8208 |
| rs748973823 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36389473 | TAGCTGGGCATGGTG[A/G]TGCGCTCCTATAATC | 8208 |
| rs749061160 | in-del | -/G | 1.65427e-05 | 0.00287595 | utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36386106 | TAGAACGGTGCCCGA[-/G]AAACGTTTTTCCCCT | 8208 |
| rs749088557 | in-del | -/AG | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36401764 | TTTGTTTGTTGAGAC[-/AG]TGTCTGGCTCTGTCA | 8208 |
| rs749101775 | snp | C/T | 3.32138e-05 | 0.00407502 | synonymous-codon, intron-variant | CHAF1B | GRCh38.p7 | 21:36397452 | TGAACATAAAAGTTA[C/T]GTCCAAGGAGTAACC | 8208 |
| rs749114612 | snp | A/G | | | | | GRCh38.p7 | 21:36377688 | GAGCAGGAGGGCATG[A/G]CACGTCCCTGTGTGC | 8208 |
| rs749146474 | snp | C/T | 6.64386e-05 | 0.00576323 | synonymous-codon | CHAF1B | GRCh38.p7 | 21:36413112 | AGACCCCAGCAGCCC[C/T]GGCACGACTCCCCCT | 8208 |
| rs749177427 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36405645 | TATGTTGCCCAGGCT[A/G]GTCTTAAACTCCTGG | 8208 |
| rs749185430 | snp | A/G | | | downstream-variant-500B | CHAF1B | GRCh38.p7 | 21:36417224 | CTACAGGCATGTGCC[A/G]CCATGCCATGCTAAT | 8208 |
| rs749195123 | snp | C/T | 1.65671e-05 | 0.00287807 | synonymous-codon | MORC3 | GRCh38.p7 | 21:36375263 | GATTTTAGGACAAGT[C/T]GTTGAACAAATGAGT | 8208 |
| rs749223042 | snp | A/T | 0.00105208 | 0.0229114 | intron-variant | CHAF1B | GRCh38.p7 | 21:36415732 | TCCCCGGCTGCTACT[A/T]CTTGCCCATGACATT | 8208 |
| rs749317564 | snp | C/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36413516 | AGTTTCTGCCTGTCA[C/G]ATAAAGCCCAGGCTC | 8208 |
| rs749390019 | snp | C/T | 3.372e-05 | 0.00410595 | synonymous-codon | CHAF1B | GRCh38.p7 | 21:36416288 | AGAGACGCCTGGAGA[C/T]GCTCAGGGCAGTCCC | 8208 |
| rs749413531 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36399726 | CGATTCCAGAACTAC[A/G]ATAAGGCTTCCTTTT | 8208 |
| rs749439006 | snp | C/T | 1.65081e-05 | 0.00287293 | intron-variant | CHAF1B | GRCh38.p7 | 21:36409345 | CTTAGTCACAGTGCC[C/T]TTTCCTAACACTGCA | 8208 |
| rs749460534 | snp | A/G | 1.6516e-05 | 0.00287362 | missense, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36391559 | CCTGCAGATGCTGTC[A/G]TCCTATTGTGGAAGG | 8208 |
| rs749471961 | snp | C/T | 1.65236e-05 | 0.00287429 | intron-variant | CHAF1B | GRCh38.p7 | 21:36409500 | GGTGTGTTATGTTTT[C/T]TCTCCGAAACAGGTC | 8208 |
| rs749536961 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36412525 | CCACCATGGCTGGCT[A/G]ATTTTTTTGTATTTG | 8208 |
| rs749576099 | in-del | -/AT | | | downstream-variant-500B | CHAF1B | GRCh38.p7 | 21:36417283 | ATATATATGATACAT[-/AT]ATATATATATATACA | 8208 |
| rs749580708 | snp | A/G | | | upstream-variant-2KB, intron-variant | CHAF1B | GRCh38.p7 | 21:36383452 | TAAAATGCCTTGAGA[A/G]GTTTTTTTTCGAAGC | 8208 |
| rs749589777 | snp | C/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36388867 | CAGTGTGCCCTCCCA[C/G]TGGCCCCTCTTCAGT | 8208 |
| rs749607233 | in-del | -/C | 0.00109769 | 0.0234018 | intron-variant | CHAF1B | GRCh38.p7 | 21:36415762 | TCTTTTTTTTTTTTT[-/C]TTTTTTTTGAGATGC | 8208 |
| rs749739766 | snp | C/T | 3.30568e-05 | 0.00406538 | intron-variant | CHAF1B | GRCh38.p7 | 21:36399638 | ATTCTTTTTCAGCAG[C/T]GCTTTAACTGAGACT | 8208 |
| rs749786288 | snp | A/G | 1.77741e-05 | 0.00298107 | missense | CHAF1B | GRCh38.p7 | 21:36413305 | CAAGCCTGGAGCAAG[A/G]CAACACCCCGGTAAG | 8208 |
| rs749847674 | snp | A/G | 3.3653e-05 | 0.00410188 | synonymous-codon | CHAF1B | GRCh38.p7 | 21:36413229 | GGAGGAGAAGACCCT[A/G]CAGCCCAGTAGTCAA | 8208 |
| rs749877526 | snp | A/C/G | 0.000230599 | 0.0107354 | missense | CHAF1B | GRCh38.p7 | 21:36411564 | TTCCCTTTTGGTTAC[A/C/G]TGTCTAATATACATT | 8208 |
| rs749891968 | snp | C/G | 1.64833e-05 | 0.00287078 | missense, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36391642 | CCAGCTGAACAAGGA[C/G]AACTGGACGGTTGTG | 8208 |
| rs749920817 | in-del | -/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36389313 | AACTATATGGAAAAA[-/G]TAAACCAGGCTGGGC | 8208 |
| rs749928560 | snp | A/T | | | downstream-variant-500B | CHAF1B | GRCh38.p7 | 21:36416924 | CATCATCTTCCCACC[A/T]GAAGTAACCCTCGTT | 8208 |
| rs749951738 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36410907 | CTCAGGTGATCTGCC[C/T]GCCTCAGTTTCCTCT | 8208 |
| rs749955171 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36397136 | CTTCTCAGACCCTCC[A/G]CCCTGTGCTGTCAGC | 8208 |
| rs750048678 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36391042 | TAGGAACATTTGCCA[A/G]CCCTTGCACTGAGGG | 8208 |
| rs750154112 | snp | C/T | | | | | GRCh38.p7 | 21:36377432 | AGTATTGCCAAGATA[C/T]GAGACTTCGAAAATG | 8208 |
| rs750292466 | in-del | -/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36383090 | CTGTTATCAAAGCTT[-/T]TTTTTTTTTTTTTTT | 8208 |
| rs750301622 | snp | C/G | 6.93361e-05 | 0.00588755 | missense | CHAF1B | GRCh38.p7 | 21:36413278 | TCCCGGAGGGTCACT[C/G]TGAACACACTGCAAG | 8208 |
| rs750325132 | snp | C/T | 1.64757e-05 | 0.00287012 | synonymous-codon | CHAF1B | GRCh38.p7 | 21:36402844 | CGGATCTTTGCTTCT[C/T]ACGCCAGGTGTGTTT | 8208 |
| rs750325153 | snp | A/T | 1.64901e-05 | 0.00287137 | missense, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36386204 | GCCTGGACTTCCAGC[A/T]TGGGACGGCTGGGAG | 8208 |
| rs750363825 | snp | C/T | | | upstream-variant-2KB, intron-variant | CHAF1B | GRCh38.p7 | 21:36383460 | CTTGAGAAGTTTTTT[C/T]TCGAAGCTGAGTTAA | 8208 |
| rs750374368 | snp | A/G | 1.67136e-05 | 0.00289076 | intron-variant | CHAF1B | GRCh38.p7 | 21:36402732 | CAAACAAAAAAAATA[A/G]TAAAAATAAATTTTG | 8208 |
| rs750410142 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36398229 | GGCTAATTTTTATAT[C/T]TTTTTGTAAAGATGG | 8208 |
| rs750540385 | snp | A/G | | | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36378216 | TGTGTGCATACATGC[A/G]CACATTCATGTGTAT | 8208 |
| rs750566740 | in-del | -/C | 1.71469e-05 | 0.002928 | intron-variant | CHAF1B | GRCh38.p7 | 21:36415260 | TGTGATACTAATGAG[-/C]CATCACCCCTCTACT | 8208 |
| rs750611514 | snp | A/G | 3.29641e-05 | 0.00405968 | missense, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36394590 | TGCTGGGCAACTGAT[A/G]GGAATTTAATGGCTT | 8208 |
| rs750697108 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36405412 | AAAACCTGCAAAATA[C/T]ATAGAGTAAATTTAT | 8208 |
| rs750736887 | in-del | -/G | | | utr-variant-3-prime | CHAF1B | GRCh38.p7 | 21:36416809 | TCTAAGGAGTTGATT[-/G]ATTAAACTTTGGAAG | 8208 |
| rs750786976 | snp | A/G | 1.66574e-05 | 0.0028859 | missense, intron-variant | CHAF1B | GRCh38.p7 | 21:36397502 | ATGTTGCTACTCTGA[A/G]CTGTGACAGGTAAAT | 8208 |
| rs750994611 | snp | A/G | | | upstream-variant-2KB, intron-variant | CHAF1B | GRCh38.p7 | 21:36385167 | TAAGTAATGGATAAT[A/G]ATAATAAATAATAAT | 8208 |
| rs751041131 | snp | C/T | | | downstream-variant-500B | MORC3 | GRCh38.p7 | 21:36376913 | CTGAGGTCGGGAGTT[C/T]AAGACCAGCCTGACT | 8208 |
| rs751075836 | snp | C/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36409640 | TTATTTATTTATTTT[C/G]AGACCAGGTTATCAG | 8208 |
| rs751076008 | snp | G/T | 1.66413e-05 | 0.0028845 | intron-variant | CHAF1B | GRCh38.p7 | 21:36394509 | GCTGCTATACCTGGG[G/T]AGTAATTGCTTTTTT | 8208 |
| rs751127310 | snp | A/C | 1.65499e-05 | 0.00287657 | intron-variant | CHAF1B | GRCh38.p7 | 21:36402752 | AATAAATTTTGTGTG[A/C]GACAGGCAAGAAGCT | 8208 |
| rs751163877 | in-del | -/AAG | 1.66918e-05 | 0.00288888 | splice-acceptor-variant | CHAF1B | GRCh38.p7 | 21:36415292 | TTTTTTTTTTAAATC[-/AAG]GAGAATAAACTTAAC | 8208 |
| rs751179599 | snp | A/T | 1.67615e-05 | 0.0028949 | intron-variant | CHAF1B | GRCh38.p7 | 21:36415286 | CTACTTTTTTTTTTT[A/T]AAATCAAGGAGAATA | 8208 |
| rs751180053 | snp | A/G | 1.76724e-05 | 0.00297252 | missense | CHAF1B | GRCh38.p7 | 21:36413300 | CACTGCAAGCCTGGA[A/G]CAAGACAACACCCCG | 8208 |
| rs751246845 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36401797 | CCAGGCTGGAGTGCA[A/G]TGGCACGATCTTGGC | 8208 |
| rs751301495 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36398163 | GCTCGAGCAATCCTC[A/G]TGCTTCAGCCCCCCA | 8208 |
| rs751306443 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36396983 | CCCTCCTCTGTACCC[A/G]TTAGCAGTTCTCAGC | 8208 |
| rs751430549 | snp | A/G | 3.29457e-05 | 0.00405854 | missense, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36387653 | TGGAATTTTTGTCCA[A/G]TCTTGCTCGTCATAC | 8208 |
| rs751436532 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36415532 | ATTGTTTAAACCCGC[C/T]GGCTGCCTGTTTACG | 8208 |
| rs751543551 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36410814 | TACAGGTGTGCGCCA[C/T]CACACCCAGCTACTT | 8208 |
| rs751567186 | in-del | -/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36397720 | TGTACTTAGTAAATC[-/T]TTTTTTTTTTTTTTT | 8208 |
| rs751622758 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36403949 | TCACACATGCAGCTG[C/T]GTGGGTGGGGCTTTA | 8208 |
| rs751633300 | in-del | -/CCCAG | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36405044 | GTGTGAGCCACTGCG[-/CCCAG]CCCCAGTAGCAAATC | 8208 |
| rs751649393 | in-del | -/G | 0.000249666 | 0.0111701 | intron-variant | CHAF1B | GRCh38.p7 | 21:36397402 | GGTGCGTGTGTGTGT[-/G]TTTTTTTTGTAGGAC | 8208 |
| rs751737240 | in-del | -/T | 0.000354578 | 0.0133103 | | | GRCh38.p7 | 21:36377517 | CATGATGTATGTACC[-/T]TTCTCTTTCTTTTGT | 8208 |
| rs751743263 | snp | C/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36406153 | AGGTGCTGTTCCAGT[C/G]GAAAAAAATCTATTA | 8208 |
| rs751754143 | snp | G/T | | | upstream-variant-2KB, intron-variant | CHAF1B | GRCh38.p7 | 21:36385161 | AAGGAATAAGTAATG[G/T]ATAATAATAATAAAT | 8208 |
| rs751794457 | snp | A/G | 1.71287e-05 | 0.00292644 | intron-variant | CHAF1B | GRCh38.p7 | 21:36397529 | AAATTCAGCTTTGGC[A/G]TTTACTTGGAATTTC | 8208 |
| rs751817066 | in-del | -/C | | | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36378491 | ATGAGGTCAGGAGAT[-/C]GAGACCATCCTGGCC | 8208 |
| rs751847865 | snp | A/C | 1.65441e-05 | 0.00287607 | missense | CHAF1B | GRCh38.p7 | 21:36413077 | AGACCGGTAGAGGGA[A/C]CCCCTGCCAGCAGAA | 8208 |
| rs751851123 | snp | C/T | | | | | GRCh38.p7 | 21:36378065 | GGTTCACGAAACAAA[C/T]GGGATCAGCATATCC | 8208 |
| rs751919262 | snp | A/G | 3.36485e-05 | 0.0041016 | utr-variant-3-prime | MORC3 | GRCh38.p7 | 21:36375319 | GTTATGTAAGATAAA[A/G]TATTTGCTCAATTCT | 8208 |
| rs751946807 | snp | A/G | 0.000340368 | 0.013041 | | | GRCh38.p7 | 21:36377512 | GCTTTCATGATGTAT[A/G]TACCTTTCTCTTTCT | 8208 |
| rs751977092 | snp | A/C/T | 3.31748e-05 | 0.00407265 | intron-variant | CHAF1B | GRCh38.p7 | 21:36415417 | GTTACTGGTTTAATA[A/C/T]AATGAAAGGTAGAGT | 8208 |
| rs752056849 | snp | A/G | 1.64974e-05 | 0.00287201 | intron-variant | CHAF1B | GRCh38.p7 | 21:36409482 | TATCCTCAGAGCCTC[A/G]GGGGTGTGTTATGTT | 8208 |
| rs752063394 | snp | A/G | 3.66676e-05 | 0.00428164 | intron-variant | CHAF1B | GRCh38.p7 | 21:36416258 | ACTTGCCAACCTTAT[A/G]TTTGTTAATGTTGCA | 8208 |
| rs752089041 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36400336 | AATATAAAATTAGCC[A/G]GGTGCATGCATGTGA | 8208 |
| rs752224555 | snp | A/C | 1.6717e-05 | 0.00289106 | intron-variant | MORC3 | GRCh38.p7 | 21:36375121 | AATGCTCATCTAATA[A/C]GTTACATATTTGTAT | 8208 |
| rs752356201 | snp | C/T | 1.64779e-05 | 0.00287031 | synonymous-codon | CHAF1B | GRCh38.p7 | 21:36408804 | AATGAATACCACTTA[C/T]GTTTTCTCCAGGAAG | 8208 |
| rs752407141 | snp | A/G | 4.9436e-05 | 0.00497148 | intron-variant | CHAF1B | GRCh38.p7 | 21:36402861 | CGCCAGGTGTGTTTC[A/G]TAGCTTTGGACTTAA | 8208 |
| rs752413431 | snp | A/G | 1.65362e-05 | 0.00287538 | missense | CHAF1B | GRCh38.p7 | 21:36415380 | CCTTCTACAGAAGAA[A/G]TTCAGTCAGGTAAGT | 8208 |
| rs752418234 | in-del | -/CT | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36397719 | TTGTACTTAGTAAAT[-/CT]TTTTTTTTTTTTTTT | 8208 |
| rs752420979 | snp | A/G | | | missense | CHAF1B | GRCh38.p7 | 21:36409399 | CATCTTCCATGTCCT[A/G]GAAAAGCCACTCTTG | 8208 |
| rs752443347 | in-del | -/T/TT | 0.413828 | 0.192316 | intron-variant | CHAF1B | GRCh38.p7 | 21:36415274 | CCATCACCCCTCTAC[-/T/TT]TTTTTTTTTTTTAAA | 8208 |
| rs752467140 | in-del | -/T | | | utr-variant-5-prime, upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36380310 | GATCTGAACCATGAC[-/T]GAATTAAGGTAATTT | 8208 |
| rs752545715 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36395982 | CCATCCTCCATCCTC[C/T]GTTCTGTCTTGTTTT | 8208 |
| rs752627920 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36410889 | TGGTTTCGAACTCCT[A/G]ACCTCAGGTGATCTG | 8208 |
| rs752655935 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36408069 | GCCCTCCCTGGTGGA[C/T]ATGAAACAGTCATAT | 8208 |
| rs752774989 | in-del | -/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36401454 | TATACATAATATATA[-/T]TTTTATATTATACAT | 8208 |
| rs752804794 | snp | A/G | 1.64732e-05 | 0.0028699 | missense | CHAF1B | GRCh38.p7 | 21:36399565 | AGCGTGTGGCTTTCA[A/G]TGTTTCGAAGATGCT | 8208 |
| rs752809855 | snp | C/G | 1.73818e-05 | 0.00294798 | utr-variant-3-prime | MORC3 | GRCh38.p7 | 21:36375345 | ATTCTTTTGGTTGTA[C/G]AGCTTTCAAAATATA | 8208 |
| rs752823949 | snp | C/T | 3.31461e-05 | 0.00407086 | missense | CHAF1B | GRCh38.p7 | 21:36415332 | AAGACGGACACTCCA[C/T]CAAGTTCTGTACCAA | 8208 |
| rs752832667 | in-del | -/A | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36396664 | TCTCAAAAAAAAAAG[-/A]AAAAAAAAAAAGGAA | 8208 |
| rs752859731 | snp | C/T | 1.67077e-05 | 0.00289026 | synonymous-codon | CHAF1B | GRCh38.p7 | 21:36413187 | CTCCATCACTCCTGC[C/T]GTCAAAAGCCCCTTG | 8208 |
| rs752862735 | snp | C/T | 1.65102e-05 | 0.00287312 | intron-variant | CHAF1B | GRCh38.p7 | 21:36399473 | TGTTTCTGTGTGAAG[C/T]ATAATTCATTTACTA | 8208 |
| rs752870978 | snp | A/G | | | missense | CHAF1B | GRCh38.p7 | 21:36416344 | ATGAAAACAAAGGAG[A/G]CACGGAAAGTCTGGA | 8208 |
| rs753065051 | snp | A/G | | | downstream-variant-500B | MORC3 | GRCh38.p7 | 21:36377045 | ACTTGAACCTGGGAG[A/G]TGGAGGTTGCAGCGA | 8208 |
| rs753096715 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36404528 | CAACCTCCGCCTCCC[A/G]GGTTCAAGCCATTCT | 8208 |
| rs753174187 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36403751 | CAGCAAGATAAGGCT[A/G]GGCATTATTGTGGCC | 8208 |
| rs753205356 | snp | A/G | 1.64827e-05 | 0.00287073 | missense, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36391668 | TTGTGAAGACTCTGC[A/G]GTAACTTGGGAGGGA | 8208 |
| rs753212082 | snp | C/T | 1.64819e-05 | 0.00287066 | missense | CHAF1B | GRCh38.p7 | 21:36411466 | CCCAACCCCCAGGTG[C/T]GGAGCTGATGAGTCT | 8208 |
| rs753281613 | snp | C/T | 0.000156043 | 0.00883159 | | | GRCh38.p7 | 21:36377492 | TGTTTAACAGAACAA[C/T]GTGGGCTTTCATGAT | 8208 |
| rs753287350 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36402123 | AAGATTAATGATTAC[C/T]AGTTTAATAATCCAC | 8208 |
| rs753332541 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36398321 | GGCCACCCAAAGTGC[C/T]AAGATTACAGGTGTG | 8208 |
| rs753345365 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36393288 | AGACAGGGTCTCACT[A/G]TGTTGCCCAGGCTGG | 8208 |
| rs753356105 | snp | A/T | 1.8892e-05 | 0.00307338 | intron-variant | CHAF1B | GRCh38.p7 | 21:36416251 | TTCATTTACTTGCCA[A/T]CCTTATGTTTGTTAA | 8208 |
| rs753383650 | snp | C/T | 1.64727e-05 | 0.00286986 | missense, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36387698 | TTGTGCGTTTTTCTC[C/T]AACTGGGGAAATTTT | 8208 |
| rs753438784 | snp | G/T | 1.64912e-05 | 0.00287147 | intron-variant | CHAF1B | GRCh38.p7 | 21:36408835 | AATCTTAAAAGGTAT[G/T]CAGTCAAGGAAATGT | 8208 |
| rs753441433 | snp | A/G | | | | | GRCh38.p7 | 21:36377821 | GGGTCATACATCATT[A/G]AGGAATCATTTAAGT | 8208 |
| rs753502442 | snp | A/G | 1.66868e-05 | 0.00288845 | intron-variant | CHAF1B | GRCh38.p7 | 21:36391514 | TATGAAGGAGTGTGG[A/G]TGAAGCGTGGATCAC | 8208 |
| rs753554254 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36412194 | TTGTAGACTCCCTGG[C/T]CATTTGGGGACTTCT | 8208 |
| rs753559381 | snp | A/G | 1.64754e-05 | 0.00287009 | missense | CHAF1B | GRCh38.p7 | 21:36409436 | GCTGCTGTCCGGTCT[A/G]CTTTGAACTGAGGCC | 8208 |
| rs753676556 | snp | C/G | 1.6473e-05 | 0.00286988 | synonymous-codon | CHAF1B | GRCh38.p7 | 21:36399581 | TGTTTCGAAGATGCT[C/G]TCTGGAATAGGGGCT | 8208 |
| rs753696512 | in-del | -/TTAC | | | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36378379 | GCTCCTAATGGTTAC[-/TTAC]TTACTTACTTACTTT | 8208 |
| rs753765854 | in-del | -/TTT | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36383088 | GTCTGTTATCAAAGC[-/TTT]TTTTTTTTTTTTTTT | 8208 |
| rs753796054 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36387112 | GGTAACAAGTTGCTC[C/T]AGAAAGAAGGCGGAG | 8208 |
| rs753897369 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36395695 | CATTCTGTTCTCTAG[C/T]TGGGGAGACAGTGGA | 8208 |
| rs753911899 | snp | A/G | 0.000136958 | 0.00827408 | utr-variant-5-prime, upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36380227 | GTGTTTTATATTCAC[A/G]AAGGAGTCAAGTCTT | 8208 |
| rs753959758 | snp | C/T | 2.26457e-05 | 0.00336487 | utr-variant-3-prime | CHAF1B | GRCh38.p7 | 21:36416413 | GGCTCCCGGTGTGTG[C/T]AGGGAGACGGTAAAG | 8208 |
| rs754039374 | snp | C/T | 1.64746e-05 | 0.00287002 | missense | CHAF1B | GRCh38.p7 | 21:36411489 | ATGAGTCTGCCCTAC[C/T]GCCTGGTGTTTGCTG | 8208 |
| rs754039790 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36394507 | AAGCTGCTATACCTG[A/G]GGAGTAATTGCTTTT | 8208 |
| rs754096788 | snp | C/T | 1.73504e-05 | 0.00294532 | synonymous-codon | CHAF1B | GRCh38.p7 | 21:36416345 | TGAAAACAAAGGAGG[C/T]ACGGAAAGTCTGGAC | 8208 |
| rs754133411 | snp | A/G | | | upstream-variant-2KB, intron-variant | CHAF1B | GRCh38.p7 | 21:36383478 | GAAGCTGAGTTAAGA[A/G]TTAGTCCCTTTATAT | 8208 |
| rs754187944 | snp | C/T | 1.65048e-05 | 0.00287265 | synonymous-codon, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36394550 | TTTGGATTCTAGGGG[C/T]CACTTAGAAGATGTG | 8208 |
| rs754193187 | snp | C/T | 1.64746e-05 | 0.00287002 | missense | CHAF1B | GRCh38.p7 | 21:36411574 | GTTACGTGTCTAATA[C/T]ACATTACCACACCCT | 8208 |
| rs754275775 | snp | C/G | 1.68872e-05 | 0.00290574 | intron-variant | CHAF1B | GRCh38.p7 | 21:36394695 | AAGAAATATTCTAAG[C/G]ATCTATAAAAGCCTA | 8208 |
| rs754280019 | in-del | -/TTAT | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36406166 | GTGGAAAAAAATCTA[-/TTAT]TTATTTGTAATTAAT | 8208 |
| rs754369744 | snp | C/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36400585 | CCTCCATGATTCTCA[C/G]GTATAGCAAGGGCTG | 8208 |
| rs754502141 | snp | A/C | 1.77071e-05 | 0.00297544 | missense | CHAF1B | GRCh38.p7 | 21:36413301 | ACTGCAAGCCTGGAG[A/C]AAGACAACACCCCGG | 8208 |
| rs754532461 | snp | C/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36412205 | CTGGCCATTTGGGGA[C/G]TTCTGAGGCCCTCTG | 8208 |
| rs754693846 | snp | C/T | | | upstream-variant-2KB, intron-variant | CHAF1B | GRCh38.p7 | 21:36383486 | GTTAAGAGTTAGTCC[C/T]TTTATATCAATTTTC | 8208 |
| rs754722891 | snp | A/C | 8.33785e-05 | 0.00645618 | intron-variant | CHAF1B | GRCh38.p7 | 21:36415292 | TTTTTTTTTTAAATC[A/C]AGGAGAATAAACTTA | 8208 |
| rs754734966 | in-del | -/ACA | 1.64817e-05 | 0.00287064 | cds-indel | CHAF1B | GRCh38.p7 | 21:36386168 | GTGAAATAGCCTGGC[-/ACA]ACAAGGAGCCCGTGT | 8208 |
| rs754738123 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36407959 | CTCCAGCCTGGGTGA[C/T]AGAGCAAGACTCCAT | 8208 |
| rs754745701 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36398334 | GCTAAGATTACAGGT[A/G]TGCTACGGTGATTTT | 8208 |
| rs754846315 | in-del | -/AGTG | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36389799 | GTGTGTGTGTGTGTG[-/AGTG]TGCGCGCGCACGCTG | 8208 |
| rs754955180 | snp | A/G | 1.64765e-05 | 0.00287019 | missense | CHAF1B | GRCh38.p7 | 21:36412998 | GCCAGTTTTGAACAT[A/G]AGAACTCCTGATACA | 8208 |
| rs754966448 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36406734 | GTGGTTTGAACGCTT[C/T]ATATCTCTTAGCATT | 8208 |
| rs755002708 | in-del | -/T | 3.30109e-05 | 0.00406256 | intron-variant | CHAF1B | GRCh38.p7 | 21:36399626 | AATATTTTGCCATTC[-/T]TTTTTCAGCAGCGCT | 8208 |
| rs755035739 | in-del | -/TCTTTTTTTTT | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36397718 | TTTGTACTTAGTAAA[-/TCTTTTTTTTT]TTTTTTTTTTTTAGA | 8208 |
| rs755045127 | snp | G/T | 1.76291e-05 | 0.00296888 | intron-variant | CHAF1B | GRCh38.p7 | 21:36397400 | TTGGTGCGTGTGTGT[G/T]TGTTTTTTTTGTAGG | 8208 |
| rs755156183 | in-del | -/T | | | upstream-variant-2KB, intron-variant | CHAF1B | GRCh38.p7 | 21:36383815 | GCCACGCCCGACTAA[-/T]TTTTTTGTAATTTTT | 8208 |
| rs755180447 | snp | C/T | 0.000132253 | 0.00813075 | synonymous-codon, stop-gained | CHAF1B | GRCh38.p7 | 21:36394646 | CATATGGGATGTCAG[C/T]AAAGGTAAATGATAT | 8208 |
| rs755198660 | snp | C/T | 0.000152177 | 0.00872156 | utr-variant-3-prime | MORC3 | GRCh38.p7 | 21:36375331 | AAAATATTTGCTCAA[C/T]TCTTTTGGTTGTACA | 8208 |
| rs755293288 | snp | G/T | 6.94843e-05 | 0.00589384 | intron-variant | CHAF1B | GRCh38.p7 | 21:36416271 | ATGTTTGTTAATGTT[G/T]CAGAGACGCCTGGAG | 8208 |
| rs755315771 | snp | A/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36389522 | GAGGTGGAGAATCGC[A/T]GTAACCTGGGAGGTG | 8208 |
| rs755331586 | snp | A/G | 1.66726e-05 | 0.00288722 | intron-variant | CHAF1B | GRCh38.p7 | 21:36408873 | GTTTACATTTTTTTT[A/G]GACGGAGTTTCGCTC | 8208 |
| rs755490056 | snp | A/G | 3.29968e-05 | 0.00406169 | intron-variant | CHAF1B | GRCh38.p7 | 21:36409483 | ATCCTCAGAGCCTCA[A/G]GGGTGTGTTATGTTT | 8208 |
| rs755548362 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36389051 | CCAGCAGTGCCGGTC[A/G]GGGTAAGATCCCGCG | 8208 |
| rs755576076 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36402269 | GCGACCTATGATTGC[A/G]CCACTGCACTCTAGC | 8208 |
| rs755621165 | snp | C/G | 3.30764e-05 | 0.00406659 | missense | CHAF1B | GRCh38.p7 | 21:36415383 | TCTACAGAAGAAATT[C/G]AGTCAGGTAAGTAAT | 8208 |
| rs755690502 | snp | C/T | 3.29451e-05 | 0.00405851 | synonymous-codon, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36387675 | TCGTCATACCAAAGC[C/T]GTCAATGTTGTGCGT | 8208 |
| rs755764232 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36409788 | CAGGTGTGAGCCCCT[A/G]TGCCCGGCCTGGTTT | 8208 |
| rs755812719 | snp | A/G/T | 3.32968e-05 | 0.00408014 | intron-variant | CHAF1B | GRCh38.p7 | 21:36386295 | TAGACATCCGGGAAC[A/G/T]CTGCTTGAAGCAATA | 8208 |
| rs755821149 | snp | A/G | 1.6477e-05 | 0.00287024 | synonymous-codon | CHAF1B | GRCh38.p7 | 21:36413022 | TGATACAGCAAAGAA[A/G]ACCAAGAGTCAGACA | 8208 |
| rs755822136 | snp | G/T | | | downstream-variant-500B | MORC3 | GRCh38.p7 | 21:36376973 | ATACAAAATTAGCCG[G/T]GTGTGGTGATGCATG | 8208 |
| rs755891784 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36410943 | CTTAAGCATATAGAG[C/T]GCAGTTATAATAGCT | 8208 |
| rs756011874 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36385937 | GCTAGCAAGGTGTTA[C/T]TGTCAGATGGCAACG | 8208 |
| rs756053961 | snp | C/T | | | upstream-variant-2KB, intron-variant | CHAF1B | GRCh38.p7 | 21:36383484 | GAGTTAAGAGTTAGT[C/T]CCTTTATATCAATTT | 8208 |
| rs756062915 | snp | A/G | | | downstream-variant-500B | CHAF1B | GRCh38.p7 | 21:36417117 | TGCTCTGTTGCCCAG[A/G]CTGGAGTGCAGTGGC | 8208 |
| rs756069732 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36398271 | GTTGCCCAGGCTGGT[C/T]GCGAACTGTTGAGCT | 8208 |
| rs756088596 | snp | C/T | 1.6473e-05 | 0.00286988 | missense | CHAF1B | GRCh38.p7 | 21:36399571 | TGGCTTTCAATGTTT[C/T]GAAGATGCTGTCTGG | 8208 |
| rs756128652 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36394411 | GATGGGATTTTACTG[C/T]GTTAGCCAGGCTGGC | 8208 |
| rs756209730 | snp | G/T | | | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36378221 | GCATACATGCACACA[G/T]TCATGTGTATGTATT | 8208 |
| rs756238279 | in-del | -/GCCCA | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36405042 | GGTGTGAGCCACTGC[-/GCCCA]GCCCAGCCCCAGTAG | 8208 |
| rs756279657 | snp | G/T | | | upstream-variant-2KB, intron-variant | CHAF1B | GRCh38.p7 | 21:36383371 | AAAGCGTTGGGATTA[G/T]AGATGTGAGCCACCA | 8208 |
| rs756305878 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36406432 | CTGGGATTACAGGCG[C/T]CGGCCACCATGCCCA | 8208 |
| rs756319367 | snp | A/T | 1.65067e-05 | 0.00287282 | intron-variant | CHAF1B | GRCh38.p7 | 21:36409494 | CTCAGGGGTGTGTTA[A/T]GTTTTCTCTCCGAAA | 8208 |
| rs756349179 | snp | C/G | 1.70324e-05 | 0.00291821 | missense | CHAF1B | GRCh38.p7 | 21:36416336 | CAGACTCGATGAAAA[C/G]AAAGGAGGCACGGAA | 8208 |
| rs756399272 | snp | A/G | 1.64814e-05 | 0.00287061 | synonymous-codon | CHAF1B | GRCh38.p7 | 21:36411467 | CCAACCCCCAGGTGT[A/G]GAGCTGATGAGTCTG | 8208 |
| rs756432284 | snp | A/G/T | 0.000271394 | 0.0116463 | utr-variant-5-prime, upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36380196 | GCTGGCTGTATCTTC[A/G/T]TAACAAAATGTAATG | 8208 |
| rs756475646 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36388074 | GTGATCCACCTGCCT[C/T]GGCCTCCCAAAGTGT | 8208 |
| rs756512203 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36398274 | GCCCAGGCTGGTCGC[A/G]AACTGTTGAGCTCAA | 8208 |
| rs756554412 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36413412 | AATTTCAGGCGGTGA[A/G]TGCTTCATGCCAGTA | 8208 |
| rs756604096 | snp | A/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36396489 | AACATGGCAAAACCC[A/T]CTCTCTACCAAAAAA | 8208 |
| rs756632312 | snp | C/T | 1.64822e-05 | 0.00287068 | intron-variant | CHAF1B | GRCh38.p7 | 21:36391673 | AAGACTCTGCGGTAA[C/T]TTGGGAGGGACCATG | 8208 |
| rs756655054 | snp | A/G | | | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36379414 | CTCCCAAATTGTTGG[A/G]ATTACAGGCATTTGA | 8208 |
| rs756730107 | snp | A/G | 3.31323e-05 | 0.00407002 | synonymous-codon | MORC3 | GRCh38.p7 | 21:36375179 | AGTTAACGTAGGACA[A/G]CTGCTGGCTATGATT | 8208 |
| rs756889046 | snp | A/C/G | 4.98371e-05 | 0.00499164 | missense | CHAF1B | GRCh38.p7 | 21:36413113 | GACCCCAGCAGCCCC[A/C/G]GCACGACTCCCCCTC | 8208 |
| rs756935581 | snp | A/G | 1.64855e-05 | 0.00287097 | intron-variant | CHAF1B | GRCh38.p7 | 21:36399506 | AGTGGTAAATCAGAC[A/G]TGTTCTTTCTTCAGG | 8208 |
| rs756972652 | in-del | -/CTGA | | | utr-variant-5-prime, intron-variant | CHAF1B | GRCh38.p7 | 21:36385430 | GAGGTGACGGTGCCT[-/CTGA]CTGTCCGGGTCCCTC | 8208 |
| rs756979003 | snp | C/T | 1.67435e-05 | 0.00289335 | missense | CHAF1B | GRCh38.p7 | 21:36413197 | CCTGCTGTCAAAAGC[C/T]CCTTGCCGGGGCCTT | 8208 |
| rs756987852 | in-del | -/AATT | 1.65373e-05 | 0.00287548 | frameshift-variant | CHAF1B | GRCh38.p7 | 21:36415378 | CCCTTCTACAGAAGA[-/AATT]AATTCAGTCAGGTAA | 8208 |
| rs756994258 | snp | G/T | 1.66621e-05 | 0.00288631 | intron-variant | CHAF1B | GRCh38.p7 | 21:36391519 | AGGAGTGTGGGTGAA[G/T]CGTGGATCACTGTTA | 8208 |
| rs757029886 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36415541 | ACCCGCCGGCTGCCT[A/G]TTTACGCCTCAGCAG | 8208 |
| rs757090988 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36410844 | TTTTTTATTTTTAGT[A/G]GAGGCAGGGTTTTGC | 8208 |
| rs757116185 | in-del | -/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36398056 | TTATTATTATTACTA[-/T]TTTTTTTTTTTTTTG | 8208 |
| rs757142242 | snp | C/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36397006 | TTCTCAGCTACCTCT[C/G]CCTGCTCCATATTCA | 8208 |
| rs757167971 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36396148 | GGGATTACAGGCGCC[C/T]GCCACCACTCCCAGC | 8208 |
| rs757184746 | snp | C/G | 0.00109409 | 0.0233634 | utr-variant-5-prime, upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36380235 | TATTCACAAAGGAGT[C/G]AAGTCTTCCTAATCT | 8208 |
| rs757207825 | snp | A/G | 1.64735e-05 | 0.00286993 | missense | CHAF1B | GRCh38.p7 | 21:36399588 | AAGATGCTGTCTGGA[A/G]TAGGGGCTGAAGGAG | 8208 |
| rs757229798 | snp | C/T | 1.64893e-05 | 0.0028713 | synonymous-codon, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36386199 | GTACAGCCTGGACTT[C/T]CAGCATGGGACGGCT | 8208 |
| rs757293974 | snp | C/G | | | intron-variant, upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36380830 | TCAAGCGATGCACTC[C/G]CCCACCTCTTAACCT | 8208 |
| rs757385095 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36405091 | GCCACTCTAAAAATA[C/T]TTTCAATTAAAATCA | 8208 |
| rs757387898 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36391368 | GTATTTTTAGTAGAG[A/G]CAGTTAGCCAGGATG | 8208 |
| rs757442115 | snp | A/G | | | utr-variant-3-prime | CHAF1B | GRCh38.p7 | 21:36416628 | AACTGGAGCGGTTCA[A/G]CGTTATCCAGTGTGA | 8208 |
| rs757466879 | snp | C/T | 1.64836e-05 | 0.0028708 | intron-variant | CHAF1B | GRCh38.p7 | 21:36391684 | GTAACTTGGGAGGGA[C/T]CATGGCAGTGATCTC | 8208 |
| rs757468123 | snp | A/G | 1.64741e-05 | 0.00286998 | missense | CHAF1B | GRCh38.p7 | 21:36411490 | TGAGTCTGCCCTACC[A/G]CCTGGTGTTTGCTGT | 8208 |
| rs757478888 | snp | C/G | | | missense | CHAF1B | GRCh38.p7 | 21:36409387 | AGGCCCATCGCTCAT[C/G]TTCCATGTCCTGGAA | 8208 |
| rs757497097 | snp | A/G | 1.6476e-05 | 0.00287014 | missense | CHAF1B | GRCh38.p7 | 21:36411575 | TTACGTGTCTAATAT[A/G]CATTACCACACCCTC | 8208 |
| rs757510298 | in-del | -/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36414600 | TGAAAATTAAGACTC[-/G]TGGGTTTTTATTTAT | 8208 |
| rs757559336 | snp | A/G | 1.64906e-05 | 0.00287142 | missense, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36394561 | GGGGCCACTTAGAAG[A/G]TGTGTATGATATTTG | 8208 |
| rs757737218 | snp | A/G | 5.00463e-05 | 0.00500206 | intron-variant | MORC3 | GRCh38.p7 | 21:36375127 | CATCTAATAAGTTAC[A/G]TATTTGTATTTGCAG | 8208 |
| rs757797814 | snp | A/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36408605 | GACAGTGCCGGAATA[A/T]ATGTTTTTGTGCTCT | 8208 |
| rs757870005 | snp | C/T | 9.88924e-05 | 0.0070311 | missense, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36391650 | ACAAGGAGAACTGGA[C/T]GGTTGTGAAGACTCT | 8208 |
| rs757938706 | snp | A/G | | | synonymous-codon | CHAF1B | GRCh38.p7 | 21:36399533 | CAGGGTGCTGCGAGT[A/G]TACAGTATACAGAAG | 8208 |
| rs758009458 | in-del | -/AAAA | 1.69331e-05 | 0.00290968 | intron-variant | CHAF1B | GRCh38.p7 | 21:36402722 | GTGTAGAAAACAAAC[-/AAAA]AAAATAATAAAAATA | 8208 |
| rs758033735 | snp | A/C | 1.64757e-05 | 0.00287012 | synonymous-codon | CHAF1B | GRCh38.p7 | 21:36399602 | AATAGGGGCTGAAGG[A/C]GAGGTATAAAATATT | 8208 |
| rs758111064 | snp | A/C | 1.67668e-05 | 0.00289537 | missense | CHAF1B | GRCh38.p7 | 21:36413209 | AGCCCCTTGCCGGGG[A/C]CTTCGGAGGAGAAGA | 8208 |
| rs758123718 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36402733 | AAACAAAAAAAATAA[C/T]AAAAATAAATTTTGT | 8208 |
| rs758207508 | in-del | -/TT | 0.00604765 | 0.0546557 | intron-variant | CHAF1B | GRCh38.p7 | 21:36415275 | CCATCACCCCTCTAC[-/TT]TTTTTTTTTTAAATC | 8208 |
| rs758272743 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36408122 | GTATCAAGAAATAGC[A/G]TAAAACAGGGAGATG | 8208 |
| rs758301606 | snp | G/T | 1.65754e-05 | 0.00287879 | intron-variant | CHAF1B | GRCh38.p7 | 21:36386273 | TCAGGGTAAACTGGG[G/T]CAGAGATAGACATCC | 8208 |
| rs758333311 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36409490 | GAGCCTCAGGGGTGT[A/G]TTATGTTTTCTCTCC | 8208 |
| rs758358794 | snp | A/G | 1.64923e-05 | 0.00287156 | missense, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36386207 | TGGACTTCCAGCATG[A/G]GACGGCTGGGAGGAT | 8208 |
| rs758396159 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36394923 | TTTTAGTAGAGACGG[A/G]TTTCATCATGTTGGC | 8208 |
| rs758423135 | in-del | -/TT | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36391908 | CTGCTGATTTTTAAA[-/TT]TTTTTTTTTTTTTTT | 8208 |
| rs758449845 | snp | A/G | 7.72753e-05 | 0.00621544 | utr-variant-3-prime | CHAF1B | GRCh38.p7 | 21:36416376 | CCTTGATGGGACCTC[A/G]GCTTCTGCTCGAAGC | 8208 |
| rs758598871 | snp | C/G | 1.6483e-05 | 0.00287076 | missense, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36394591 | GCTGGGCAACTGATG[C/G]GAATTTAATGGCTTC | 8208 |
| rs758630463 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36414779 | ACCATGCCTGGCTGA[C/T]TTTTTGCATTTTTAG | 8208 |
| rs758643366 | snp | C/T | 1.79567e-05 | 0.00299634 | intron-variant | CHAF1B | GRCh38.p7 | 21:36397389 | GTAATGCTGTTTTGG[C/T]GCGTGTGTGTGTGTT | 8208 |
| rs758705531 | snp | C/T | | | downstream-variant-500B | MORC3 | GRCh38.p7 | 21:36377110 | ACAAGAGCGAAACTC[C/T]GTCTCAAAAAAAAAG | 8208 |
| rs758735375 | snp | C/T | 1.65663e-05 | 0.002878 | synonymous-codon | MORC3 | GRCh38.p7 | 21:36375180 | GTTAACGTAGGACAA[C/T]TGCTGGCTATGATTG | 8208 |
| rs758735762 | in-del | -/AG | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36397570 | CTTGGAATTTTCTGA[-/AG]AGAGGTATTTATCGT | 8208 |
| rs758745075 | snp | G/T | 1.64909e-05 | 0.00287144 | missense | CHAF1B | GRCh38.p7 | 21:36412938 | CGGTTACTGCTCATT[G/T]GTGACATTTGAGAAA | 8208 |
| rs758755493 | in-del | -/ATC | 1.6585e-05 | 0.00287962 | cds-indel | MORC3 | GRCh38.p7 | 21:36375282 | GAACAAATGAGTGAA[-/ATC]AGTAGTACTTAAAGT | 8208 |
| rs758819628 | snp | A/C | 6.60982e-05 | 0.00574846 | intron-variant | CHAF1B | GRCh38.p7 | 21:36408847 | TATGCAGTCAAGGAA[A/C]TGTTTGAAATGTTTA | 8208 |
| rs758864266 | snp | A/C | | | intron-variant, upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36380788 | ATTTTTGACTTGTTG[A/C]CCAGGCTGGTCTCAA | 8208 |
| rs758888290 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36403860 | CAGGGTTGGGCCAAA[C/T]GGGAGGGCACTGTCT | 8208 |
| rs758943946 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36414163 | TTCCATTCTTCCCCT[A/G]CAGCTGATGTCCAGT | 8208 |
| rs758947597 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36391182 | TTTAAGGTGATTTTG[C/T]ATAGCTCTGATCTGT | 8208 |
| rs759104366 | snp | C/T | 1.6623e-05 | 0.00288292 | intron-variant | CHAF1B | GRCh38.p7 | 21:36394661 | CAAAGGTAAATGATA[C/T]ATTTTTGTTATTAGC | 8208 |
| rs759111630 | snp | A/G | 1.67332e-05 | 0.00289246 | intron-variant | MORC3 | GRCh38.p7 | 21:36375117 | TTGTAATGCTCATCT[A/G]ATAAGTTACATATTT | 8208 |
| rs759297500 | snp | A/C/T | 1.65682e-05 | 0.00287817 | missense, synonymous-codon | CHAF1B | GRCh38.p7 | 21:36413100 | CAGCAGAACCCAAGA[A/C/T]CCCAGCAGCCCCGGC | 8208 |
| rs759312928 | snp | C/T | | | utr-variant-3-prime | MORC3 | GRCh38.p7 | 21:36375839 | TGTCCTGAAATATTT[C/T]ATTCATGAAAATAAG | 8208 |
| rs759313703 | snp | A/G | 3.29544e-05 | 0.00405908 | missense | CHAF1B | GRCh38.p7 | 21:36408790 | TCTGGTGAAAATGTA[A/G]TGAATACCACTTATG | 8208 |
| rs759349931 | snp | A/G | 0.000304321 | 0.0123316 | intron-variant | CHAF1B | GRCh38.p7 | 21:36415878 | CTGCCTCGGCCTCCC[A/G]AGTAGCCGGGACTAC | 8208 |
| rs759361557 | in-del | -/CTT | 6.80284e-05 | 0.00583177 | intron-variant | CHAF1B | GRCh38.p7 | 21:36415274 | GCCATCACCCCTCTA[-/CTT]TTTTTTTTTTAAATC | 8208 |
| rs759365462 | snp | C/G | 1.64838e-05 | 0.00287083 | intron-variant | CHAF1B | GRCh38.p7 | 21:36387769 | ATTCTTCGGGAACCA[C/G]ATAGATACCTGTGTG | 8208 |
| rs759420528 | snp | A/G | 3.29587e-05 | 0.00405934 | missense | CHAF1B | GRCh38.p7 | 21:36409381 | TCCATTAGGCCCATC[A/G]CTCATCTTCCATGTC | 8208 |
| rs759530480 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36400882 | TTACTGGCTTCACAC[A/G]GGGACATGGTGCAAA | 8208 |
| rs759548731 | snp | G/T | 0.000131776 | 0.00811608 | missense, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36387658 | TTTTTGTCCAATCTT[G/T]CTCGTCATACCAAAG | 8208 |
| rs759589101 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36395201 | ACTACAGGTGTCTGC[C/T]ACCACACCTGGCTAA | 8208 |
| rs759607604 | in-del | -/C | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36407940 | CCAAGATCACGCCAT[-/C]GCACTCCAGCCTGGG | 8208 |
| rs759707417 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36408947 | GCAACCTCTGCCTCC[C/T]GGGTTCAAGTGATTC | 8208 |
| rs759756509 | snp | A/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36410610 | CTCATCTCTAGAGAT[A/T]CACTTTGGGTTTTCC | 8208 |
| rs759766318 | in-del | -/T | | | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36379135 | CCACAGTAGGTTGTC[-/T]TTTTTTTTTTTTTTT | 8208 |
| rs759798573 | snp | G/T | 1.64732e-05 | 0.0028699 | missense | CHAF1B | GRCh38.p7 | 21:36399558 | CAGAAGAAGCGTGTG[G/T]CTTTCAATGTTTCGA | 8208 |
| rs759822351 | snp | C/T | 1.67086e-05 | 0.00289033 | synonymous-codon | CHAF1B | GRCh38.p7 | 21:36413172 | CATCAGGGACCCTCC[C/T]TCCATCACTCCTGCT | 8208 |
| rs759875419 | in-del | -/GT | 0.167244 | 0.235905 | intron-variant | CHAF1B | GRCh38.p7 | 21:36397392 | ATGCTGTTTTGGTGC[-/GT]GTGTGTGTGTTTTTT | 8208 |
| rs760011506 | snp | C/G | | | upstream-variant-2KB, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36384540 | GCTTCCTGTAGAAAT[C/G]AGGCTTCAAGGAGCA | 8208 |
| rs760031631 | snp | A/G | 1.68332e-05 | 0.00290109 | synonymous-codon | CHAF1B | GRCh38.p7 | 21:36416324 | GCTAAAGCGGCCCAG[A/G]CTCGATGAAAACAAA | 8208 |
| rs760033114 | snp | A/G | 1.65444e-05 | 0.00287609 | intron-variant | CHAF1B | GRCh38.p7 | 21:36399651 | AGCGCTTTAACTGAG[A/G]CTTAGGAAGTCATGA | 8208 |
| rs760035260 | snp | A/C | 0.000178811 | 0.00945375 | | | GRCh38.p7 | 21:36377522 | TGTATGTACCTTTCT[A/C]TTTCTTTTGTTGCAT | 8208 |
| rs760081380 | snp | G/T | 1.68439e-05 | 0.00290201 | missense | CHAF1B | GRCh38.p7 | 21:36416326 | TAAAGCGGCCCAGAC[G/T]CGATGAAAACAAAGG | 8208 |
| rs760088106 | snp | A/C | 1.64904e-05 | 0.00287139 | intron-variant | CHAF1B | GRCh38.p7 | 21:36411455 | TTGTCTCTGTCCCCA[A/C]CCCCCAGGTGTGGAG | 8208 |
| rs760111981 | snp | C/T | | | | | GRCh38.p7 | 21:36377794 | TGCTGTCACATGAGA[C/T]GTCTTAAACTTGGGT | 8208 |
| rs760123435 | snp | A/G | 3.3006e-05 | 0.00406226 | utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36386124 | ACGTTTTTCCCCTTC[A/G]AGACTCAGGAGGATG | 8208 |
| rs760209562 | in-del | -/TATT | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36409622 | TTTTACATTTAAATC[-/TATT]TATTTATTTATTTTG | 8208 |
| rs760231668 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36412044 | CAATTTTGTTTTTTA[A/G]AGGAATCAACATTAA | 8208 |
| rs760328655 | snp | A/G | 0.000148093 | 0.00860376 | | | GRCh38.p7 | 21:36377472 | GTTGCAGACAGAACA[A/G]CTGTTGTTTAACAGA | 8208 |
| rs760337298 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36405677 | CTCAAGCACCCCTTC[C/T]GCCTCGGCCTCCCAA | 8208 |
| rs760372569 | snp | A/C/G | 3.29496e-05 | 0.00405881 | synonymous-codon | CHAF1B | GRCh38.p7 | 21:36409431 | TGTTCGCTGCTGTCC[A/C/G]GTCTACTTTGAACTG | 8208 |
| rs760428304 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36388388 | AGTTTAACATCTGTG[A/G]TGATCAGAGTCAGTT | 8208 |
| rs760489240 | snp | G/T | 3.30748e-05 | 0.00406649 | intron-variant | CHAF1B | GRCh38.p7 | 21:36411422 | CCTGGTCAGAAGCCT[G/T]GTTTCTGTGGTTTTA | 8208 |
| rs760502373 | snp | C/G | 1.672e-05 | 0.00289132 | synonymous-codon | CHAF1B | GRCh38.p7 | 21:36413190 | CATCACTCCTGCTGT[C/G]AAAAGCCCCTTGCCG | 8208 |
| rs760522489 | snp | A/G | 5.01458e-05 | 0.00500704 | missense | CHAF1B | GRCh38.p7 | 21:36413188 | TCCATCACTCCTGCT[A/G]TCAAAAGCCCCTTGC | 8208 |
| rs760574559 | snp | G/T | 3.29609e-05 | 0.00405948 | intron-variant | CHAF1B | GRCh38.p7 | 21:36387781 | CCAGATAGATACCTG[G/T]GTGTCTTGTGTCAGA | 8208 |
| rs760778057 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36412845 | TAGATGTGAGAGTGT[C/T]GGTAAGGTCTGTAAC | 8208 |
| rs760784933 | snp | C/G | 1.64743e-05 | 0.00287 | missense | CHAF1B | GRCh38.p7 | 21:36402822 | GTAGACTGAGTTTCA[C/G]TCCCGACGGATCTTT | 8208 |
| rs760786249 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36408607 | CAGTGCCGGAATATA[C/T]GTTTTTGTGCTCTGT | 8208 |
| rs760938509 | in-del | -/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36403481 | AAAAAAAAAAAAAAA[-/G]AAACTTTACTATTTA | 8208 |
| rs760987630 | snp | C/G | 1.6795e-05 | 0.0028978 | intron-variant | CHAF1B | GRCh38.p7 | 21:36402712 | TAAGCTTTGTGTGTA[C/G]AAAACAAACAAAAAA | 8208 |
| rs760997288 | snp | G/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36415029 | AAGACCGTCGGTAAT[G/T]AACAGAACACAGGTT | 8208 |
| rs761138163 | snp | C/T | 1.70784e-05 | 0.00292214 | synonymous-codon | CHAF1B | GRCh38.p7 | 21:36412890 | GGGACGAAGGTCCAG[C/T]GATGGTGCCTTCCTG | 8208 |
| rs761186456 | snp | A/G | 6.61244e-05 | 0.0057496 | missense, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36386248 | GCGTCTGCCGGCGTG[A/G]ACACCAATGTCAGGG | 8208 |
| rs761206007 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36395629 | TGCATGCTAGTTGAT[A/G]GGGTAGGTGGGATCA | 8208 |
| rs761298518 | snp | A/C | 1.65384e-05 | 0.00287557 | utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36386107 | AGAACGGTGCCCGAG[A/C]AACGTTTTTCCCCTT | 8208 |
| rs761388978 | in-del | -/A | | | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36379417 | CAAATTGTTGGGATT[-/A]ACAGGCATTTGAGCC | 8208 |
| rs761396555 | snp | C/G | 1.65037e-05 | 0.00287256 | intron-variant | CHAF1B | GRCh38.p7 | 21:36411446 | GGTTTTACTTTGTCT[C/G]TGTCCCCAACCCCCA | 8208 |
| rs761462671 | snp | A/C | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36403087 | TTTGGAATTTTAAGA[A/C]GATTTCCAAGTGATT | 8208 |
| rs761487122 | snp | A/G | | | downstream-variant-500B | MORC3 | GRCh38.p7 | 21:36376915 | GAGGTCGGGAGTTCA[A/G]GACCAGCCTGACTAA | 8208 |
| rs761492606 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36412657 | GTGAGCCACCGCACC[C/T]GGCCTATTCAAGTGA | 8208 |
| rs761526218 | snp | G/T | 1.64852e-05 | 0.00287094 | missense, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36391632 | AGGACGAGGCCCAGC[G/T]GAACAAGGAGAACTG | 8208 |
| rs761535156 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36389483 | TGGTGGTGCGCTCCT[A/G]TAATCCTAGCTACTC | 8208 |
| rs761736785 | snp | G/T | 1.91269e-05 | 0.00309242 | intron-variant | CHAF1B | GRCh38.p7 | 21:36413363 | AAATGAAACACAAAA[G/T]GCAGACAGAACGCTC | 8208 |
| rs761748483 | in-del | -/TT | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36383089 | TCTGTTATCAAAGCT[-/TT]TTTTTTTTTTTTTTT | 8208 |
| rs761762874 | snp | C/T | 1.64996e-05 | 0.0028722 | intron-variant | CHAF1B | GRCh38.p7 | 21:36391715 | TGTTTACGATGAGTG[C/T]ATTAAATGGAATATA | 8208 |
| rs761768464 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36407554 | TCAATAAAAAATATC[A/G]TAGAGGTATACATGT | 8208 |
| rs761788231 | snp | C/T | 0.000481133 | 0.0155027 | missense | CHAF1B | GRCh38.p7 | 21:36413266 | AAAGCCCACCCATCC[C/T]GGAGGGTCACTCTGA | 8208 |
| rs761811748 | in-del | -/TTTTTTTTTTTTCTTGCTCTGTTGCC | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36410677 | TCTTGCTGCTTTCTT[-/TTTTTTTTTTTTCTTGCTCTGTTGCC]CAGGCTGGGGTGCAG | 8208 |
| rs761823048 | snp | A/G | 1.64746e-05 | 0.00287002 | missense | CHAF1B | GRCh38.p7 | 21:36402828 | TGAGTTTCACTCCCG[A/G]CGGATCTTTGCTTCT | 8208 |
| rs761858109 | snp | C/T | | | | | GRCh38.p7 | 21:36377751 | GTCCAGTTGGTGACG[C/T]TGCCTGTGATCTCAG | 8208 |
| rs761878678 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36411925 | GTAGAGATGGGGTTT[C/T]GCCCTGTTGGCCAGG | 8208 |
| rs761905633 | snp | A/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36398761 | TGGCATAATTGCATT[A/T]AATTGTATTGTTGGA | 8208 |
| rs761959074 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36406214 | ATAATTCTCAAGAGA[A/G]TTAGACACTGAAGGC | 8208 |
| rs762039478 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36386687 | TTCCAGGGCCTGCGG[C/T]GAACAATGAAAGCAA | 8208 |
| rs762055649 | snp | C/T | 1.65048e-05 | 0.00287265 | intron-variant | CHAF1B | GRCh38.p7 | 21:36408741 | TTTTCTTTCCTCTCC[C/T]TCCCTTCCCTGTTCC | 8208 |
| rs762129577 | snp | A/G | 1.65499e-05 | 0.00287657 | missense, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36386260 | GTGGACACCAATGTC[A/G]GGGTAAACTGGGGCA | 8208 |
| rs762257041 | snp | A/G | 3.8449e-05 | 0.0043844 | intron-variant | CHAF1B | GRCh38.p7 | 21:36397366 | TATTTGGGCTCAAAC[A/G]GGTTTTGGTAATGCT | 8208 |
| rs762259665 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36395477 | AGGCTTAGCACTGGT[A/G]CTGCAAGTTACTGAT | 8208 |
| rs762339778 | in-del | -/GA | | | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36378359 | AACATTTCATCATAG[-/GA]ATATGCTCCTAATGG | 8208 |
| rs762352356 | snp | A/G | 1.65847e-05 | 0.0028796 | missense, intron-variant | CHAF1B | GRCh38.p7 | 21:36397487 | ACCCTTTGGGTCAAT[A/G]TGTTGCTACTCTGAG | 8208 |
| rs762353531 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36401065 | TGAGGTCAGGAGTTC[A/G]AGACTAGCCTGGCTA | 8208 |
| rs762367975 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36407715 | GGGTGCAGTGACTCA[C/T]GCCTGTAATCCCAGC | 8208 |
| rs762395659 | snp | A/G | 4.94173e-05 | 0.00497053 | synonymous-codon | CHAF1B | GRCh38.p7 | 21:36411542 | TCTGTATGACACCCA[A/G]CAGTCCTTCCCTTTT | 8208 |
| rs762405550 | snp | C/T | 3.29962e-05 | 0.00406165 | missense | CHAF1B | GRCh38.p7 | 21:36413065 | TCGCCAGGACCCAGA[C/T]CGGTAGAGGGAACCC | 8208 |
| rs762419325 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36394289 | ACCATGTTGGCCAGG[A/G]TGGTCTCGATCTCCC | 8208 |
| rs762528085 | snp | A/C | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36394024 | CCTGCCTCAGCCCCC[A/C]AGTAGCAGGGACTAC | 8208 |
| rs762541500 | snp | A/G | 1.66576e-05 | 0.00288592 | intron-variant | CHAF1B | GRCh38.p7 | 21:36394502 | GGGGTAAGCTGCTAT[A/G]CCTGGGGAGTAATTG | 8208 |
| rs762597021 | snp | C/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36414986 | ACCATATCTGACTGC[C/G]TTTTACAGCAGCCAG | 8208 |
| rs762642304 | snp | A/G | 1.64898e-05 | 0.00287135 | missense, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36394618 | CTTCTGCCTCTGTGG[A/G]TAACACAGCCATCAT | 8208 |
| rs762787464 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36410804 | TAGCCAGGATTACAG[A/G]TGTGCGCCACCACAC | 8208 |
| rs762817251 | snp | A/G | 1.65474e-05 | 0.00287636 | missense | CHAF1B | GRCh38.p7 | 21:36415351 | GTTCTGTACCAACCA[A/G]TGTGATTTCCACCCC | 8208 |
| rs762848564 | snp | G/T | 1.64866e-05 | 0.00287106 | intron-variant | CHAF1B | GRCh38.p7 | 21:36408754 | CCCTCCCTTCCCTGT[G/T]CCCCAGCTGGATGTG | 8208 |
| rs762871723 | snp | C/G | 1.67654e-05 | 0.00289524 | intron-variant | MORC3 | GRCh38.p7 | 21:36375112 | TTAACTTGTAATGCT[C/G]ATCTAATAAGTTACA | 8208 |
| rs762904226 | snp | C/T | 8.23784e-05 | 0.00641735 | missense | CHAF1B | GRCh38.p7 | 21:36402846 | GATCTTTGCTTCTCA[C/T]GCCAGGTGTGTTTCG | 8208 |
| rs762957244 | snp | A/T | | | upstream-variant-2KB, intron-variant | CHAF1B | GRCh38.p7 | 21:36384885 | TAAAATGTTAGTCTG[A/T]TCTTAAAAAGGGTTT | 8208 |
| rs763065593 | snp | C/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36386594 | CAGAGCCAGACCCTT[C/G]TCTTAAGTAAATGAA | 8208 |
| rs763164194 | snp | C/T | 8.23839e-05 | 0.00641757 | intron-variant | CHAF1B | GRCh38.p7 | 21:36387760 | CCTTCAGAGATTCTT[C/T]GGGAACCAGATAGAT | 8208 |
| rs763172228 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36397927 | GAGACAGGGTTTCAC[C/T]ACGTTGGTCAAGCTG | 8208 |
| rs763173450 | snp | A/T | 1.68647e-05 | 0.0029038 | intron-variant | CHAF1B | GRCh38.p7 | 21:36397518 | CTGTGACAGGTAAAT[A/T]CAGCTTTGGCATTTA | 8208 |
| rs763204174 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36382733 | ATTTTTGAGATGGAG[C/T]TCTGCTCTTGTTGCC | 8208 |
| rs763212463 | snp | C/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36392958 | ACTCTGTCTGCAATC[C/G]CGGCACCTCGGGAGG | 8208 |
| rs763241499 | in-del | -/T | 0.000347205 | 0.0131713 | intron-variant | CHAF1B | GRCh38.p7 | 21:36397393 | TGCTGTTTTGGTGCG[-/T]GTGTGTGTGTTTTTT | 8208 |
| rs763288547 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36390309 | TTGCACTCCAGCCTG[A/G]GCAATAAGAGTGAAA | 8208 |
| rs763340739 | snp | C/T | | | | | GRCh38.p7 | 21:36377900 | CCCAAAGTCAGGCTG[C/T]ACCTCACGTTAATTA | 8208 |
| rs763354487 | snp | A/G | 1.66849e-05 | 0.00288828 | missense | CHAF1B | GRCh38.p7 | 21:36413146 | GCCAGACAGGCCCCA[A/G]CCCCAACAGTCATCA | 8208 |
| rs763373186 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36407063 | TCCCAGCACTCTGGG[A/G]GGCCAAGGTGGGTGG | 8208 |
| rs763442527 | in-del | -/C | 8.25621e-05 | 0.0064245 | intron-variant | CHAF1B | GRCh38.p7 | 21:36411616 | CATGGTGAGTGGCTG[-/C]TAATGAGGGAGAGTG | 8208 |
| rs763466523 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36404885 | AGTAGCTGAGATTAC[A/G]GGCGCCTGCCACCAC | 8208 |
| rs763502573 | snp | C/T | 1.88032e-05 | 0.00306614 | intron-variant | CHAF1B | GRCh38.p7 | 21:36416252 | TCATTTACTTGCCAA[C/T]CTTATGTTTGTTAAT | 8208 |
| rs763545777 | snp | C/T | 3.30786e-05 | 0.00406672 | missense | CHAF1B | GRCh38.p7 | 21:36415387 | CAGAAGAAATTCAGT[C/T]AGGTAAGTAATATTG | 8208 |
| rs763557316 | snp | A/C | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36405967 | AGTATTAAAAAAAAA[A/C]CAGTGATACTTGGGA | 8208 |
| rs763611356 | snp | A/G | 3.3543e-05 | 0.00409516 | utr-variant-3-prime | MORC3 | GRCh38.p7 | 21:36375311 | AAGTATATGTTATGT[A/G]AGATAAAATATTTGC | 8208 |
| rs763611888 | in-del | -/AGG | | | intron-variant, cds-indel | CHAF1B | GRCh38.p7 | 21:36381767 | TGCAAGAGATTGATC[-/AGG]AGGAGTGGCTTAAGT | 8208 |
| rs763637649 | snp | C/G | 3.86153e-05 | 0.00439388 | intron-variant | CHAF1B | GRCh38.p7 | 21:36416247 | ATTCTTCATTTACTT[C/G]CCAACCTTATGTTTG | 8208 |
| rs763647096 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36400432 | GCTGAAATCACACCA[C/T]TGCACTCCAGCCTGG | 8208 |
| rs763675229 | snp | C/T | 1.64795e-05 | 0.00287045 | missense | CHAF1B | GRCh38.p7 | 21:36408811 | ACCACTTATGTTTTC[C/T]CCAGGAAGAATCTTA | 8208 |
| rs763686705 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36389445 | ACCTCATCTCTACTA[A/G]AAATACAAAAATTAG | 8208 |
| rs763700127 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36388756 | ACAGGCGTGAGCCAC[C/T]GCGCCCGGGCTATTT | 8208 |
| rs763739045 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36390405 | AACCTCATTCATTCA[C/T]TGTCCTGCTGTGCAC | 8208 |
| rs763776247 | in-del | -/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36410670 | TTTTCCTCTTGCTGC[-/T]TTTCTTTTTTTTTTT | 8208 |
| rs763853248 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36401715 | TATGAATAGTAATGC[C/T]GGCTTCCTTGTGTTC | 8208 |
| rs763895686 | snp | A/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36396932 | ACACAAGGTCTCTGT[A/T]ATACTTCTCCTTTCC | 8208 |
| rs763933534 | snp | C/T | 8.24559e-05 | 0.00642037 | synonymous-codon, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36391621 | TTTTCAGGATGAGGA[C/T]GAGGCCCAGCTGAAC | 8208 |
| rs763992472 | snp | A/G | 5.03124e-05 | 0.00501534 | intron-variant | CHAF1B | GRCh38.p7 | 21:36391500 | AATAAAAATCCTAAT[A/G]TGAAGGAGTGTGGGT | 8208 |
| rs764029869 | snp | C/T | 1.67942e-05 | 0.00289772 | intron-variant | CHAF1B | GRCh38.p7 | 21:36402717 | TTTGTGTGTAGAAAA[C/T]AAACAAAAAAAATAA | 8208 |
| rs764075222 | snp | C/T | 8.35708e-05 | 0.00646362 | missense | CHAF1B | GRCh38.p7 | 21:36413189 | CCATCACTCCTGCTG[C/T]CAAAAGCCCCTTGCC | 8208 |
| rs764117401 | snp | C/T | | | intron-variant | MORC3 | GRCh38.p7 | 21:36375087 | TTACTTTTTAAGGTC[C/T]ACATGAATCTTAACT | 8208 |
| rs764135821 | snp | C/T | | | downstream-variant-500B | MORC3 | GRCh38.p7 | 21:36376676 | ATATTAACCTCAAAT[C/T]ATTTTAAAACTAAAA | 8208 |
| rs764225603 | snp | A/T | | | utr-variant-3-prime | CHAF1B | GRCh38.p7 | 21:36416518 | GTGTACTGATTTTTC[A/T]CCAGAAATATGGATG | 8208 |
| rs764238425 | snp | A/G | 3.29457e-05 | 0.00405854 | synonymous-codon | CHAF1B | GRCh38.p7 | 21:36399572 | GGCTTTCAATGTTTC[A/G]AAGATGCTGTCTGGA | 8208 |
| rs764298757 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36383220 | CAGCCTCCCTAGTAT[C/T]CCGAGTAGCTGGGAT | 8208 |
| rs764317218 | snp | C/T | | | upstream-variant-2KB, intron-variant | CHAF1B | GRCh38.p7 | 21:36385080 | TCCAAGTGCCCAGCG[C/T]CAGCATAGGGTCTGT | 8208 |
| rs764394407 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36394184 | CAGGTTCAAGTGATT[C/T]CCCTCCCTCACCCTC | 8208 |
| rs764450433 | in-del | -/T | 0.000141015 | 0.00839569 | intron-variant | CHAF1B | GRCh38.p7 | 21:36397400 | TGGTGCGTGTGTGTG[-/T]TGTTTTTTTTGTAGG | 8208 |
| rs764534792 | snp | C/G | 1.65395e-05 | 0.00287567 | synonymous-codon, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36386253 | TGCCGGCGTGGACAC[C/G]AATGTCAGGGTAAAC | 8208 |
| rs764563107 | snp | G/T | | | | | GRCh38.p7 | 21:36377932 | GTCAGCGTCCTTGGG[G/T]TTAGACCCAGATAAC | 8208 |
| rs764652184 | snp | C/T | 3.30715e-05 | 0.00406628 | intron-variant | CHAF1B | GRCh38.p7 | 21:36394536 | TTTTCCTCTTTGTTT[C/T]TGGATTCTAGGGGCC | 8208 |
| rs764686164 | snp | C/T | 1.64893e-05 | 0.0028713 | intron-variant | CHAF1B | GRCh38.p7 | 21:36409470 | GGTGGAAACAGGTAT[C/T]CTCAGAGCCTCAGGG | 8208 |
| rs764785182 | snp | C/T | 4.94898e-05 | 0.00497418 | intron-variant | CHAF1B | GRCh38.p7 | 21:36411450 | TTACTTTGTCTCTGT[C/T]CCCAACCCCCAGGTG | 8208 |
| rs764786375 | snp | A/T | | | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36379232 | GCTTACTGCAGCCTC[A/T]ACCTCCGAGGCCCAA | 8208 |
| rs764958082 | snp | A/G | 1.64993e-05 | 0.00287218 | intron-variant | CHAF1B | GRCh38.p7 | 21:36391716 | GTTTACGATGAGTGC[A/G]TTAAATGGAATATAC | 8208 |
| rs764977362 | snp | A/C | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36414251 | CCATAAACTGAGTCA[A/C]GAGGAGAGCTGGGAA | 8208 |
| rs764986563 | snp | A/G | 6.87521e-05 | 0.00586271 | missense | CHAF1B | GRCh38.p7 | 21:36413267 | AAGCCCACCCATCCC[A/G]GAGGGTCACTCTGAA | 8208 |
| rs765053500 | snp | A/G | 1.6483e-05 | 0.00287076 | missense, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36391638 | AGGCCCAGCTGAACA[A/G]GGAGAACTGGACGGT | 8208 |
| rs765151295 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36410810 | GGATTACAGGTGTGC[A/G]CCACCACACCCAGCT | 8208 |
| rs765185475 | snp | A/G | 1.65553e-05 | 0.00287705 | splice-donor-variant | CHAF1B | GRCh38.p7 | 21:36386263 | GACACCAATGTCAGG[A/G]TAAACTGGGGCAGAG | 8208 |
| rs765193022 | in-del | -/T | 0.0147193 | 0.0845163 | intron-variant | CHAF1B | GRCh38.p7 | 21:36415275 | CCATCACCCCTCTAC[-/T]TTTTTTTTTTTAAAT | 8208 |
| rs765198363 | snp | A/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36388685 | TCAGCCAGGCTGGTC[A/T]CAAACTCCTGAGCTC | 8208 |
| rs765219296 | snp | A/G | 1.91896e-05 | 0.00309749 | intron-variant | CHAF1B | GRCh38.p7 | 21:36413364 | AATGAAACACAAAAT[A/G]CAGACAGAACGCTCC | 8208 |
| rs765274966 | snp | C/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36383174 | GCTCACTGCAACCTC[C/G]AAGTCCCGGGTTCAA | 8208 |
| rs765367431 | snp | A/G | 3.2981e-05 | 0.00406071 | synonymous-codon, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36386202 | CAGCCTGGACTTCCA[A/G]CATGGGACGGCTGGG | 8208 |
| rs765440182 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36395890 | TTGTTGGCTGCCACC[A/G]CAGCACTGTGTCAGC | 8208 |
| rs765540008 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36405680 | AAGCACCCCTTCCGC[C/T]TCGGCCTCCCAAAGA | 8208 |
| rs765542655 | snp | G/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36388699 | CTCAAACTCCTGAGC[G/T]CAGGCAATCTGCCTG | 8208 |
| rs765615392 | snp | A/G | 1.90127e-05 | 0.00308318 | intron-variant | CHAF1B | GRCh38.p7 | 21:36397368 | TTTGGGCTCAAACAG[A/G]TTTTGGTAATGCTGT | 8208 |
| rs765680834 | in-del | -/G | | | | | GRCh38.p7 | 21:36377533 | TCTCTTTCTTTTGTT[-/G]GCATGTGGGGGACAG | 8208 |
| rs765690516 | in-del | -/GT | 0.167244 | 0.235905 | intron-variant | CHAF1B | GRCh38.p7 | 21:36397391 | ATGCTGTTTTGGTGC[-/GT]GTGTGTGTGTGTTTT | 8208 |
| rs765730723 | snp | C/T | 1.66222e-05 | 0.00288285 | synonymous-codon, intron-variant | CHAF1B | GRCh38.p7 | 21:36397498 | CAATATGTTGCTACT[C/T]TGAGCTGTGACAGGT | 8208 |
| rs765861890 | snp | C/G | 6.66345e-05 | 0.00577172 | intron-variant | CHAF1B | GRCh38.p7 | 21:36394504 | GGTAAGCTGCTATAC[C/G]TGGGGAGTAATTGCT | 8208 |
| rs765874633 | snp | G/T | 3.29451e-05 | 0.00405851 | missense | CHAF1B | GRCh38.p7 | 21:36411556 | AGCAGTCCTTCCCTT[G/T]TGGTTACGTGTCTAA | 8208 |
| rs765944350 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36382466 | TTACACTTCCACCAG[C/T]AGTGTGCCAGAGGTC | 8208 |
| rs765979617 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36401515 | TATTTTTATATTATA[C/T]ATAATATATATTTTT | 8208 |
| rs766001040 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36398308 | ATCTGTCTGCCTTGG[C/T]CACCCAAAGTGCTAA | 8208 |
| rs766004730 | snp | G/T | | | synonymous-codon | CHAF1B | GRCh38.p7 | 21:36412905 | CGATGGTGCCTTCCT[G/T]GCCATTTCTTCCACG | 8208 |
| rs766015489 | snp | A/T | | | downstream-variant-500B | MORC3 | GRCh38.p7 | 21:36377008 | TAATCCCAGCTACTC[A/T]GGAGGCTGAGGCAGG | 8208 |
| rs766034177 | snp | G/T | | | | | GRCh38.p7 | 21:36377819 | TTGGGTCATACATCA[G/T]TGAGGAATCATTTAA | 8208 |
| rs766276447 | snp | A/C | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36387103 | TTCCTACTGGGTAAC[A/C]AGTTGCTCTAGAAAG | 8208 |
| rs766281141 | in-del | -/T | 0.000720974 | 0.0189728 | intron-variant | CHAF1B | GRCh38.p7 | 21:36397403 | GTGCGTGTGTGTGTG[-/T]TTTTTTTGTAGGACA | 8208 |
| rs766363139 | in-del | -/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36395026 | ATGAACCACTGCCCC[-/T]GGCCCTAACTTACCT | 8208 |
| rs766365466 | in-del | -/TG | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36389763 | GCATGAAGGGATGTG[-/TG]TGTGTGTGTGTGTGT | 8208 |
| rs766392970 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36395652 | TGGGATCAGGTTTCC[A/G]TTTTAGAAGATCAAG | 8208 |
| rs766410029 | snp | A/T | 1.64817e-05 | 0.00287064 | synonymous-codon | CHAF1B | GRCh38.p7 | 21:36408765 | CTGTTCCCCAGCTGG[A/T]TGTGTGGAATCTGGT | 8208 |
| rs766457791 | snp | C/T | 3.29462e-05 | 0.00405857 | synonymous-codon, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36387646 | GCCATCGTGGAATTT[C/T]TGTCCAATCTTGCTC | 8208 |
| rs766514273 | snp | G/T | | | utr-variant-5-prime, intron-variant | CHAF1B | GRCh38.p7 | 21:36385404 | CGCGGGAAGCGGCGC[G/T]CGCTGCGCGGGAGGT | 8208 |
| rs766537328 | snp | A/G | 1.64844e-05 | 0.00287087 | missense | CHAF1B | GRCh38.p7 | 21:36412948 | TCATTTGTGACATTT[A/G]AGAAAGATGAACTTG | 8208 |
| rs766640650 | in-del | -/CTAAAGTTTTTTTTTGC | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36389681 | AAATAAAACAGAAAT[-/CTAAAGTTTTTTTTTGC]CTAAAGTTTTTTTTT | 8208 |
| rs766718623 | snp | A/G | 3.36231e-05 | 0.00410005 | utr-variant-3-prime | MORC3 | GRCh38.p7 | 21:36375318 | TGTTATGTAAGATAA[A/G]ATATTTGCTCAATTC | 8208 |
| rs766726904 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36415107 | TGTGATGGTTTAACT[C/T]AATACATGAATGTAA | 8208 |
| rs766736644 | snp | C/T | 1.87152e-05 | 0.00305896 | intron-variant | CHAF1B | GRCh38.p7 | 21:36416253 | CATTTACTTGCCAAC[C/T]TTATGTTTGTTAATG | 8208 |
| rs766768506 | snp | A/G | 3.30251e-05 | 0.00406343 | missense | CHAF1B | GRCh38.p7 | 21:36413075 | CCAGACCGGTAGAGG[A/G]AACCCCTGCCAGCAG | 8208 |
| rs766775614 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36414655 | CTTGCTCTGTTGCCC[A/G]GGCTGGAGTGCGATG | 8208 |
| rs766785193 | in-del | -/GCAGCCCAGTAGTCAAAACAC | 0.00124272 | 0.024896 | cds-indel | CHAF1B | GRCh38.p7 | 21:36413229 | GGAGGAGAAGACCCT[-/GCAGCCCAGTAGTCAAAACAC]AAAAGCCCACCCATC | 8208 |
| rs766837718 | snp | A/G | 0.000816393 | 0.0201874 | | | GRCh38.p7 | 21:36377503 | ACAACGTGGGCTTTC[A/G]TGATGTATGTACCTT | 8208 |
| rs766859242 | snp | C/T | 1.6968e-05 | 0.00291268 | intron-variant | CHAF1B | GRCh38.p7 | 21:36397522 | GACAGGTAAATTCAG[C/T]TTTGGCATTTACTTG | 8208 |
| rs766946573 | snp | C/G | | | utr-variant-3-prime | CHAF1B | GRCh38.p7 | 21:36416683 | CCTCGTGAAAGTGCA[C/G]ACACTTCATGGAGGG | 8208 |
| rs766970964 | snp | A/G | 1.67284e-05 | 0.00289205 | intron-variant | MORC3 | GRCh38.p7 | 21:36375118 | TGTAATGCTCATCTA[A/G]TAAGTTACATATTTG | 8208 |
| rs767026566 | snp | C/T | 1.66827e-05 | 0.00288809 | intron-variant | CHAF1B | GRCh38.p7 | 21:36394673 | ATATATTTTTGTTAT[C/T]AGCAGGAAGAAATAT | 8208 |
| rs767100652 | snp | A/C | 1.66418e-05 | 0.00288455 | missense | CHAF1B | GRCh38.p7 | 21:36415304 | ATCAAGGAGAATAAA[A/C]TTAACACCCTTAAAG | 8208 |
| rs767147374 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36410881 | GGCCAGTCTGGTTTC[A/G]AACTCCTGACCTCAG | 8208 |
| rs767153141 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36403111 | AGTGATTGTAATGTG[C/T]AGAAAAGTTTGGGAG | 8208 |
| rs767204152 | snp | A/G | 1.66713e-05 | 0.0028871 | utr-variant-3-prime | MORC3 | GRCh38.p7 | 21:36375300 | AGTAGTACTTAAAGT[A/G]TATGTTATGTAAGAT | 8208 |
| rs767206606 | in-del | -/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36396002 | GTCTTGTTTTGTGTG[-/T]GTTTTTTTTTTTATT | 8208 |
| rs767252771 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36393073 | GAAAACCAGACAGGC[A/G]TGGCGGCGTGCGCCT | 8208 |
| rs767292980 | snp | C/T | 1.64746e-05 | 0.00287002 | synonymous-codon | CHAF1B | GRCh38.p7 | 21:36409410 | TCCTGGAAAAGCCAC[C/T]CTTGCTGTTCGCTGC | 8208 |
| rs767339595 | snp | A/G | 1.65367e-05 | 0.00287543 | synonymous-codon | CHAF1B | GRCh38.p7 | 21:36415373 | TTCCACCCCTTCTAC[A/G]GAAGAAATTCAGTCA | 8208 |
| rs767370904 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36399160 | CTGCCTCAGCCTCCC[A/G]AGTAGCAGGGATTAC | 8208 |
| rs767397765 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36398201 | GGGACTACGGGTGTG[C/T]ACCACCACACCCGGC | 8208 |
| rs767469369 | snp | C/T | 0.000167023 | 0.00913694 | missense | CHAF1B | GRCh38.p7 | 21:36413174 | TCAGGGACCCTCCCT[C/T]CATCACTCCTGCTGT | 8208 |
| rs767472910 | snp | C/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36390692 | ACAGGGTCTTGCTCT[C/G]TCACTGAGGCTAGAG | 8208 |
| rs767483714 | in-del | -/AC | 1.88692e-05 | 0.00307152 | intron-variant | CHAF1B | GRCh38.p7 | 21:36413355 | TCATTGCAAAATGAA[-/AC]ACAAAATGCAGACAG | 8208 |
| rs767662979 | snp | C/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36407695 | TGGGATGAAAAGAGG[C/G]GCCTGGGTGCAGTGA | 8208 |
| rs767663024 | snp | A/T | 1.65559e-05 | 0.00287709 | missense | CHAF1B | GRCh38.p7 | 21:36413097 | TGCCAGCAGAACCCA[A/T]GACCCCAGCAGCCCC | 8208 |
| rs767714386 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36386800 | CTTACTGCAACCTCT[A/G]TCTCCCAGGTTCAAG | 8208 |
| rs767914372 | snp | C/T | 1.64732e-05 | 0.0028699 | synonymous-codon | CHAF1B | GRCh38.p7 | 21:36399563 | GAAGCGTGTGGCTTT[C/T]AATGTTTCGAAGATG | 8208 |
| rs767953331 | snp | G/T | 1.64849e-05 | 0.00287092 | missense, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36386144 | TCAGGAGGATGAAAG[G/T]CATCACTTGTGAAAT | 8208 |
| rs768006531 | snp | G/T | 0.000977039 | 0.0220809 | | | GRCh38.p7 | 21:36377538 | TTTCTTTTGTTGCAT[G/T]TGGGGGACAGTATTG | 8208 |
| rs768015697 | snp | A/C | 9.90262e-05 | 0.00703586 | intron-variant | CHAF1B | GRCh38.p7 | 21:36399626 | AAATATTTTGCCATT[A/C]TTTTTCAGCAGCGCT | 8208 |
| rs768030950 | snp | C/T | | | intron-variant, upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36380742 | ACACACCACTATGCC[C/T]AGCTAATTTTCGTAT | 8208 |
| rs768068670 | snp | A/G | 1.67863e-05 | 0.00289704 | missense | CHAF1B | GRCh38.p7 | 21:36413221 | GGGCCTTCGGAGGAG[A/G]AGACCCTGCAGCCCA | 8208 |
| rs768073624 | snp | A/G | 0.000115366 | 0.00759405 | missense | CHAF1B | GRCh38.p7 | 21:36411465 | CCCCAACCCCCAGGT[A/G]TGGAGCTGATGAGTC | 8208 |
| rs768114533 | snp | A/G | 0.000148555 | 0.00861717 | | | GRCh38.p7 | 21:36377475 | GCAGACAGAACAACT[A/G]TTGTTTAACAGAACA | 8208 |
| rs768177637 | snp | A/T | | | downstream-variant-500B | CHAF1B | GRCh38.p7 | 21:36417279 | CACACATATATATGA[A/T]ACATATATATATATA | 8208 |
| rs768229253 | snp | G/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36403508 | TTTAAACCCTTTCAA[G/T]GAATGCTTTTTCATT | 8208 |
| rs768250753 | snp | C/T | 1.6766e-05 | 0.00289529 | missense | CHAF1B | GRCh38.p7 | 21:36416316 | CCCCCAGAGCTAAAG[C/T]GGCCCAGACTCGATG | 8208 |
| rs768339344 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36416046 | GGCGTGAGCCACCGC[A/G]CCCAGCTTGCCCATG | 8208 |
| rs768347310 | snp | C/G | 0.00013709 | 0.00827804 | intron-variant, upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36380347 | AGAATTTTTTCTGTT[C/G]TAGGCAATTGTCTCT | 8208 |
| rs768407255 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36382697 | CCATGCCTGGCTGTT[A/G]TTATTATTATTATTA | 8208 |
| rs768454611 | snp | A/G | | | | | GRCh38.p7 | 21:36377700 | ATGGCACGTCCCTGT[A/G]TGCTTCCTTTGGGCC | 8208 |
| rs768501505 | snp | A/C/G | 6.06733e-05 | 0.00550759 | utr-variant-3-prime | CHAF1B | GRCh38.p7 | 21:36416387 | CCTCGGCTTCTGCTC[A/C/G]AAGCCTACCAGGCTC | 8208 |
| rs768517811 | snp | A/C | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36411809 | TCTCGTTTCACTGCA[A/C]CCTCCACCTCCCAGG | 8208 |
| rs768576314 | snp | A/G | 1.6528e-05 | 0.00287467 | intron-variant | CHAF1B | GRCh38.p7 | 21:36411431 | AAGCCTTGTTTCTGT[A/G]GTTTTACTTTGTCTC | 8208 |
| rs768673012 | snp | C/T | 1.86701e-05 | 0.00305528 | intron-variant | CHAF1B | GRCh38.p7 | 21:36413341 | GTTGGAACAAGATGT[C/T]ATTGCAAAATGAAAC | 8208 |
| rs768692182 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36412606 | ACCTCAAATGATACA[C/T]CTGCCTTGGCCTCCC | 8208 |
| rs768713060 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36405682 | GCACCCCTTCCGCCT[C/T]GGCCTCCCAAAGAGC | 8208 |
| rs768758780 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36386633 | TTAACGTATGTCAAC[A/G]AACTAAACTACTTTG | 8208 |
| rs768865946 | snp | A/G | 1.65364e-05 | 0.0028754 | intron-variant | CHAF1B | GRCh38.p7 | 21:36387565 | ATATGTGCCCATTCT[A/G]TGTTTTTCAAATGAA | 8208 |
| rs768917269 | snp | A/G | 1.65765e-05 | 0.00287888 | intron-variant | CHAF1B | GRCh38.p7 | 21:36408720 | ACAGTTTGCTGAAAC[A/G]GTGACTTTTCTTTCC | 8208 |
| rs768934400 | snp | C/T | 1.65759e-05 | 0.00287883 | missense | CHAF1B | GRCh38.p7 | 21:36415330 | TAAAGACGGACACTC[C/T]ACCAAGTTCTGTACC | 8208 |
| rs768948362 | in-del | -/CCAGCAGAACCCAAGACC | 1.65179e-05 | 0.00287379 | cds-indel | CHAF1B | GRCh38.p7 | 21:36413084 | TAGAGGGAACCCCTG[-/CCAGCAGAACCCAAGACC]CCAGCAGCCCCGGCA | 8208 |
| rs768999931 | snp | C/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36392835 | CAGAGGCTGCAATCT[C/G]AGCACTTTGGGAGGC | 8208 |
| rs769044950 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36409747 | AAGTGATCCACCTGC[C/T]TCGGCCTCCCAAAAT | 8208 |
| rs769097789 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36388188 | AGGTAGTTCAGTAAA[A/G]TACTGTTCTAGGGAA | 8208 |
| rs769146493 | in-del | -/C | 1.67598e-05 | 0.00289476 | frameshift-variant | CHAF1B | GRCh38.p7 | 21:36416301 | GACGCTCAGGGCAGT[-/C]CCCCAGAGCTAAAGC | 8208 |
| rs769209371 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36414919 | TGCCCGGCCCAACGC[C/T]CTGGATTTTAAAAAA | 8208 |
| rs769332540 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36407393 | AAAAAATACTCATTA[A/G]CAGAGGCTGGGTGAA | 8208 |
| rs769376058 | in-del | -/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36391908 | CTGCTGATTTTTAAA[-/T]TTTTTTTTTTTTTTT | 8208 |
| rs769425757 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36395413 | AGTAGGTGGTTGGCT[C/T]AACAGGATAGGGGTT | 8208 |
| rs769547801 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36400885 | CTGGCTTCACACGGG[A/G]ACATGGTGCAAATGC | 8208 |
| rs769593368 | snp | G/T | 0.000494552 | 0.0157172 | missense, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36394608 | AATTTAATGGCTTCT[G/T]CCTCTGTGGATAACA | 8208 |
| rs769624298 | snp | C/T | | | downstream-variant-500B | MORC3 | GRCh38.p7 | 21:36376710 | TATTCATTAGACCCT[C/T]AACTTGAGCTCATTT | 8208 |
| rs769648284 | snp | A/G | 3.63491e-05 | 0.00426301 | intron-variant | CHAF1B | GRCh38.p7 | 21:36412835 | CTCTTCTAAGTAGAT[A/G]TGAGAGTGTTGGTAA | 8208 |
| rs769676631 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36390226 | TAGTCCCAGCTATTC[A/G]GGAGGCTGAGGCAGG | 8208 |
| rs769697438 | in-del | -/TT | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36387224 | ATAAGCATAGTTTTG[-/TT]TTTTTTTTTTTTTTT | 8208 |
| rs769820029 | snp | A/T | 0.000164989 | 0.00908116 | intron-variant | CHAF1B | GRCh38.p7 | 21:36408742 | TTTCTTTCCTCTCCC[A/T]CCCTTCCCTGTTCCC | 8208 |
| rs769823299 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36402916 | TCTGCTCCCGTTTTA[C/T]GCTGCAGCTTATCAG | 8208 |
| rs769847323 | snp | A/G | 1.65647e-05 | 0.00287786 | missense | MORC3 | GRCh38.p7 | 21:36375244 | ATGTTGATGTAGTTG[A/G]TGAGATTTTAGGACA | 8208 |
| rs769859918 | snp | A/G | 1.65941e-05 | 0.00288041 | intron-variant | CHAF1B | GRCh38.p7 | 21:36415421 | CTGGTTTAATATAAT[A/G]AAAGGTAGAGTATCT | 8208 |
| rs769902446 | snp | A/G | 1.68142e-05 | 0.00289945 | intron-variant | MORC3 | GRCh38.p7 | 21:36375094 | TTAAGGTCTACATGA[A/G]TCTTAACTTGTAATG | 8208 |
| rs769908345 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36389210 | AGCATACCGGGAGTG[C/T]CATTAATGAATGGCC | 8208 |
| rs769945020 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36392079 | ACCCAGTGGCCTTCC[A/G]CAGTGTTTGTGTCCC | 8208 |
| rs770047177 | snp | A/G | 1.65231e-05 | 0.00287424 | intron-variant | CHAF1B | GRCh38.p7 | 21:36409323 | TTACCTTTTATTTTT[A/G]CTTTTGCTTAGTCAC | 8208 |
| rs770075369 | snp | A/G | 1.65239e-05 | 0.00287431 | missense, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36391553 | AATCACCCTGCAGAT[A/G]CTGTCATCCTATTGT | 8208 |
| rs770084947 | in-del | -/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36399977 | GAGGTCAGGAGTTTG[-/T]AGACCAGCCTGGCCA | 8208 |
| rs770095096 | snp | A/T | 6.58968e-05 | 0.00573969 | synonymous-codon, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36387618 | GAAGGTAGAAAAGGG[A/T]CCAGATGGAAAAGCC | 8208 |
| rs770122231 | snp | C/T | | | utr-variant-3-prime | MORC3 | GRCh38.p7 | 21:36376000 | GGCCACCAAGTTTAC[C/T]TTGAAGCCCATTTTT | 8208 |
| rs770224642 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36398610 | GGTGACCTGCCTGCG[C/T]TGGCCTCCCAAAGTG | 8208 |
| rs770269326 | in-del | -/GTGTGC | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36389797 | TGTGTGTGTGTGTGT[-/GTGTGC]GCGCGCACGCTGATT | 8208 |
| rs770355851 | in-del | -/T | 1.67295e-05 | 0.00289214 | intron-variant | CHAF1B | GRCh38.p7 | 21:36402730 | AACAAACAAAAAAAA[-/T]AATAAAAATAAATTT | 8208 |
| rs770376072 | snp | C/T | 7.0109e-05 | 0.00592027 | intron-variant | CHAF1B | GRCh38.p7 | 21:36412879 | TCCCTGTTTTGGGGA[C/T]GAAGGTCCAGCGATG | 8208 |
| rs770383592 | in-del | -/TT | 0.0127383 | 0.0787839 | intron-variant | CHAF1B | GRCh38.p7 | 21:36415749 | TTGCCCATGACATTC[-/TT]TTTTTTTTTTTCTTT | 8208 |
| rs770390056 | snp | C/T | | | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36378950 | ACATTTGTCTCAGTC[C/T]TTACATTGGCCATTT | 8208 |
| rs770401834 | in-del | -/TATT | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36409625 | ACATTTAAATCTATT[-/TATT]TATTTATTTATTTTG | 8208 |
| rs770469336 | in-del | -/T | 0.000351373 | 0.01325 | intron-variant | CHAF1B | GRCh38.p7 | 21:36408865 | TTTGAAATGTTTACA[-/T]TTTTTTTAGACGGAG | 8208 |
| rs770525899 | snp | A/G | 1.65021e-05 | 0.00287241 | missense | CHAF1B | GRCh38.p7 | 21:36394634 | TAACACAGCCATCAT[A/G]TGGGATGTCAGCAAA | 8208 |
| rs770547998 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36408171 | TATGATGGTCACTCT[A/G]ACAGGGCTGAACTGT | 8208 |
| rs770603858 | snp | A/G | 1.65855e-05 | 0.00287967 | synonymous-codon, intron-variant | CHAF1B | GRCh38.p7 | 21:36397458 | TAAAAGTTATGTCCA[A/G]GGAGTAACCTGGGAC | 8208 |
| rs770607149 | snp | A/G | 3.29669e-05 | 0.00405984 | missense | CHAF1B | GRCh38.p7 | 21:36413042 | AGAGTCAGACACATC[A/G]AGGGTCTTCGCCAGG | 8208 |
| rs770614304 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36409001 | GTGGGATTACAGGTG[C/T]CCGCCACCACTCCTA | 8208 |
| rs770791614 | snp | G/T | 0.000673514 | 0.0183386 | | | GRCh38.p7 | 21:36377422 | AAGATATTGAAGTAT[G/T]GCCAAGATATGAGAC | 8208 |
| rs770835886 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36380158 | CAAAATGCTGGGATT[A/G]CAGGCGTGAGCCATC | 8208 |
| rs770844547 | snp | C/T | 0.492397 | 0.0611864 | intron-variant | CHAF1B | GRCh38.p7 | 21:36415762 | TCTTTTTTTTTTTTT[C/T]TTTTTTTTGAGATGC | 8208 |
| rs770924488 | snp | A/C | 1.64917e-05 | 0.00287151 | intron-variant | CHAF1B | GRCh38.p7 | 21:36409359 | CTTTTCCTAACACTG[A/C]AATTAATCCATTAGG | 8208 |
| rs770954589 | snp | A/G | 6.59076e-05 | 0.00574016 | intron-variant | CHAF1B | GRCh38.p7 | 21:36387761 | CTTCAGAGATTCTTC[A/G]GGAACCAGATAGATA | 8208 |
| rs770990580 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36414031 | CCCAGGAGGTGCAGA[A/G]TCGTTTCTTCCCTGC | 8208 |
| rs771041993 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36400173 | CGACAGAGCGAGACT[C/T]GATTTCAAAAATAAA | 8208 |
| rs771059574 | snp | A/G | 3.36797e-05 | 0.0041035 | missense | CHAF1B | GRCh38.p7 | 21:36416289 | GAGACGCCTGGAGAC[A/G]CTCAGGGCAGTCCCC | 8208 |
| rs771131961 | snp | G/T | | | upstream-variant-2KB, intron-variant | CHAF1B | GRCh38.p7 | 21:36383581 | AAATGGATGCTTGGG[G/T]CCCAAGCTGAACAAC | 8208 |
| rs771187491 | snp | A/G | 1.65127e-05 | 0.00287334 | synonymous-codon, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36391564 | AGATGCTGTCATCCT[A/G]TTGTGGAAGGTGAAT | 8208 |
| rs771214493 | snp | C/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36416130 | CCCCTGGTTGAGAGC[C/G]ACTCTATAGAACTTC | 8208 |
| rs771249427 | in-del | -/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36391481 | AAAAAAAAAAAAAAA[-/T]GAAAATAAAAATCCT | 8208 |
| rs771344252 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36390162 | AACATGGAGAAACCT[C/T]GTCTCTACTAAAAAT | 8208 |
| rs771368910 | snp | G/T | 3.36717e-05 | 0.00410302 | missense | CHAF1B | GRCh38.p7 | 21:36413232 | GGAGAAGACCCTGCA[G/T]CCCAGTAGTCAAAAC | 8208 |
| rs771398554 | snp | A/C | | | synonymous-codon, intron-variant | CHAF1B | GRCh38.p7 | 21:36397455 | ACATAAAAGTTATGT[A/C]CAAGGAGTAACCTGG | 8208 |
| rs771403110 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36396747 | CTAAATATTTTCCCC[A/G]AAGTCCCTTTTCCAT | 8208 |
| rs771423311 | in-del | -/CT | 1.64814e-05 | 0.00287061 | frameshift-variant, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36391662 | GGACGGTTGTGAAGA[-/CT]CTGCGGTAACTTGGG | 8208 |
| rs771430207 | snp | C/T | 1.66874e-05 | 0.0028885 | missense | CHAF1B | GRCh38.p7 | 21:36413150 | GACAGGCCCCAGCCC[C/T]AACAGTCATCAGGGA | 8208 |
| rs771435098 | snp | A/G | 1.66396e-05 | 0.00288436 | synonymous-codon | CHAF1B | GRCh38.p7 | 21:36413118 | CAGCAGCCCCGGCAC[A/G]ACTCCCCCTCAGGCC | 8208 |
| rs771454096 | snp | A/C | 1.65384e-05 | 0.00287557 | utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36386110 | ACGGTGCCCGAGAAA[A/C]GTTTTTCCCCTTCGA | 8208 |
| rs771529035 | snp | C/T | 3.3151e-05 | 0.00407117 | missense, intron-variant | CHAF1B | GRCh38.p7 | 21:36397475 | GAGTAACCTGGGACC[C/T]TTTGGGTCAATATGT | 8208 |
| rs771597728 | in-del | -/AAAAG | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36390333 | GTGAAACACCATCTC[-/AAAAG]AAAAAAAAAAAAAAA | 8208 |
| rs771603711 | snp | A/G | 3.30557e-05 | 0.00406531 | intron-variant | CHAF1B | GRCh38.p7 | 21:36399639 | TTCTTTTTCAGCAGC[A/G]CTTTAACTGAGACTT | 8208 |
| rs771604291 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36406978 | AAGGAAATATAGGAG[A/G]ACATTCTAGGAATGG | 8208 |
| rs771613291 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36403873 | AACGGGAGGGCACTG[C/T]CTTGGTTTGCCACTG | 8208 |
| rs771625691 | snp | C/T | 1.64887e-05 | 0.00287125 | missense | CHAF1B | GRCh38.p7 | 21:36413053 | CATCGAGGGTCTTCG[C/T]CAGGACCCAGACCGG | 8208 |
| rs771646567 | in-del | -/TTT | | | intron-variant, upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36381115 | TCTTCTTCTTCTTTT[-/TTT]TTTTTTTTTTTTTTT | 8208 |
| rs771653029 | in-del | -/TAA | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36408014 | CTATGTAGAATGTAT[-/TAA]TAATAATAATAATAA | 8208 |
| rs771656595 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36406177 | TCTATTATTTATTTG[C/T]AATTAATTGTATGTT | 8208 |
| rs771705555 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36386412 | AGGATCGCTTGAGTC[C/T]AGGAGTTCGACACCA | 8208 |
| rs771753643 | snp | A/C | 4.94319e-05 | 0.00497127 | missense | CHAF1B | GRCh38.p7 | 21:36399525 | TCTTTCTTCAGGGTG[A/C]TGCGAGTATACAGTA | 8208 |
| rs771761741 | in-del | -/AGAT | 1.64807e-05 | 0.00287055 | intron-variant | CHAF1B | GRCh38.p7 | 21:36387768 | GATTCTTCGGGAACC[-/AGAT]AGATACCTGTGTGTC | 8208 |
| rs771761779 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36405540 | GTTCAGGGAATCCTC[C/T]CACCTCAGCCTCCCT | 8208 |
| rs771889105 | snp | A/G | 1.65004e-05 | 0.00287227 | synonymous-codon, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36391594 | TGATAACAAGGAGCC[A/G]GAGCAGATCGCTTTT | 8208 |
| rs771889270 | snp | C/G | | | | | GRCh38.p7 | 21:36377766 | CTGCCTGTGATCTCA[C/G]ACGCTTGATTCTTGC | 8208 |
| rs771998626 | snp | A/C | 0.000152451 | 0.00872938 | intron-variant | CHAF1B | GRCh38.p7 | 21:36415884 | CGGCCTCCCGAGTAG[A/C]CGGGACTACAGGCGT | 8208 |
| rs772119946 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36399959 | TGAGGTGGGCGGATC[A/G]CTTGAGGTCAGGAGT | 8208 |
| rs772122350 | snp | A/G | 1.64849e-05 | 0.00287092 | intron-variant | CHAF1B | GRCh38.p7 | 21:36391689 | TTGGGAGGGACCATG[A/G]CAGTGATCTCTGTTT | 8208 |
| rs772161324 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36389104 | CTCTGGTTTGACATC[C/T]GTGTGTTTTCTCCCA | 8208 |
| rs772176190 | snp | C/T | 1.65611e-05 | 0.00287755 | intron-variant | CHAF1B | GRCh38.p7 | 21:36411413 | GCCATTGCACCTGGT[C/T]AGAAGCCTTGTTTCT | 8208 |
| rs772176349 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36412717 | CGACTTAGCAAATCG[C/T]GATGAAACTGCATGA | 8208 |
| rs772242737 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36388288 | CCGCAAGCTCCCACC[A/G]GGCTGTTCTAAGACG | 8208 |
| rs772334780 | snp | C/G | 3.69174e-05 | 0.0042962 | intron-variant | CHAF1B | GRCh38.p7 | 21:36413330 | GGTAAGAACTTGTTG[C/G]AACAAGATGTCATTG | 8208 |
| rs772524408 | snp | A/T | 1.64757e-05 | 0.00287012 | missense | CHAF1B | GRCh38.p7 | 21:36402797 | GACGACAGCATGAAG[A/T]CTTTCTTCCGTAGAC | 8208 |
| rs772670670 | snp | A/G | 3.62733e-05 | 0.00425856 | intron-variant | CHAF1B | GRCh38.p7 | 21:36412841 | TAAGTAGATGTGAGA[A/G]TGTTGGTAAGGTCTG | 8208 |
| rs772699844 | snp | A/T | 1.67508e-05 | 0.00289398 | intron-variant | CHAF1B | GRCh38.p7 | 21:36386309 | CACTGCTTGAAGCAA[A/T]AGTTTTCATTCTTTT | 8208 |
| rs772745921 | snp | C/T | 2.13195e-05 | 0.00326485 | utr-variant-3-prime | CHAF1B | GRCh38.p7 | 21:36416401 | CGAAGCCTACCAGGC[C/T]CCCGGTGTGTGCAGG | 8208 |
| rs772757255 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36395522 | AATCCCACATGGTGG[A/G]GCCAGCAGATAAGAT | 8208 |
| rs772769980 | snp | C/T | 1.64727e-05 | 0.00286986 | synonymous-codon | CHAF1B | GRCh38.p7 | 21:36411536 | CGTGCTTCTGTATGA[C/T]ACCCAGCAGTCCTTC | 8208 |
| rs772810675 | snp | A/G/T | 0.000115613 | 0.00760224 | synonymous-codon, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36386235 | GATCCACAGACTGGC[A/G/T]TCTGCCGGCGTGGAC | 8208 |
| rs772826198 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36399184 | GGATTACAGGCGCCC[A/G]CCACCACGCCCGGCT | 8208 |
| rs772903179 | snp | C/T | 1.64879e-05 | 0.00287118 | missense, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36394609 | ATTTAATGGCTTCTG[C/T]CTCTGTGGATAACAC | 8208 |
| rs772971138 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36404210 | GTTTCAAGCGATTCT[C/T]CTGCCTCAGCCTCCT | 8208 |
| rs773040098 | snp | A/G | 1.94162e-05 | 0.00311572 | intron-variant | CHAF1B | GRCh38.p7 | 21:36413367 | GAAACACAAAATGCA[A/G]ACAGAACGCTCCCAC | 8208 |
| rs773086969 | snp | C/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36413779 | CTGTTTGCAGTCTTT[C/G]TGGCCCTTCAGCCTT | 8208 |
| rs773109303 | snp | G/T | 1.67626e-05 | 0.002895 | intron-variant | MORC3 | GRCh38.p7 | 21:36375111 | CTTAACTTGTAATGC[G/T]CATCTAATAAGTTAC | 8208 |
| rs773126089 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36389135 | TTCCCTGCTGTGACT[A/G]ATGCTGCTTTGGAGT | 8208 |
| rs773126589 | snp | A/C | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36400099 | TGAGAATCACCTGAA[A/C]CTGGGAGGCGGAGGT | 8208 |
| rs773163731 | snp | A/T | 1.65567e-05 | 0.00287716 | missense | CHAF1B | GRCh38.p7 | 21:36415342 | CTCCACCAAGTTCTG[A/T]ACCAACCAGTGTGAT | 8208 |
| rs773276566 | snp | A/T | 1.64732e-05 | 0.0028699 | missense, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36387630 | GGGACCAGATGGAAA[A/T]GCCATCGTGGAATTT | 8208 |
| rs773318276 | snp | A/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36412752 | GTCGCTATCACACAC[A/T]CTTTTCCAGTTGTAT | 8208 |
| rs773340709 | snp | A/G | 1.65652e-05 | 0.0028779 | missense | MORC3 | GRCh38.p7 | 21:36375256 | TTGATGAGATTTTAG[A/G]ACAAGTTGTTGAACA | 8208 |
| rs773462562 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36388352 | CAAGCAAGGCGACTG[C/T]TCTGGTTTTGTTGGA | 8208 |
| rs773643658 | snp | C/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36412611 | AAATGATACACCTGC[C/G]TTGGCCTCCCAAAGT | 8208 |
| rs773663896 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36396522 | ACAAAAATTAGCTGG[A/G]TGTGGTAGTACATGC | 8208 |
| rs773686411 | snp | C/T | | | intron-variant, upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36380785 | CAGATTTTTGACTTG[C/T]TGCCCAGGCTGGTCT | 8208 |
| rs773796299 | snp | C/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36403012 | TTCAAAAAACACATT[C/G]GTGCCTATGTCCCAT | 8208 |
| rs773818038 | in-del | -/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36394080 | TTTTTTTTTGGCTAA[-/T]TTTTTTTTTTTTTTT | 8208 |
| rs773827257 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36395577 | GGAGGTTAGGATCTC[A/G]GGAAGATTAACAAGT | 8208 |
| rs773845071 | snp | C/T | 1.64868e-05 | 0.00287109 | missense | CHAF1B | GRCh38.p7 | 21:36413051 | CACATCGAGGGTCTT[C/T]GCCAGGACCCAGACC | 8208 |
| rs773922596 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36405334 | AAATTCCTATCTTTC[A/G]TCTATATTGGCAGTG | 8208 |
| rs773935139 | snp | A/C/G | 3.31489e-05 | 0.00407107 | missense, intron-variant | CHAF1B | GRCh38.p7 | 21:36397474 | GGAGTAACCTGGGAC[A/C/G]CTTTGGGTCAATATG | 8208 |
| rs773981516 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36390635 | CAATTTAATCCTCAC[A/G]ACAGCCTGTGAGGTA | 8208 |
| rs773996882 | snp | C/T | 1.67405e-05 | 0.00289309 | intron-variant | MORC3 | GRCh38.p7 | 21:36375116 | CTTGTAATGCTCATC[C/T]AATAAGTTACATATT | 8208 |
| rs774001386 | snp | C/T | 1.64781e-05 | 0.00287033 | synonymous-codon | CHAF1B | GRCh38.p7 | 21:36408786 | GGAATCTGGTGAAAA[C/T]GTAATGAATACCACT | 8208 |
| rs774040578 | snp | A/G | 1.66158e-05 | 0.0028823 | missense | MORC3 | GRCh38.p7 | 21:36375289 | TGAGTGAAATCAGTA[A/G]TACTTAAAGTATATG | 8208 |
| rs774077321 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36397939 | CACCACGTTGGTCAA[A/G]CTGTTCTCAAACTCC | 8208 |
| rs774263329 | snp | G/T | 1.64727e-05 | 0.00286986 | missense, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36391575 | TCCTATTGTGGAAGG[G/T]GAATGATAACAAGGA | 8208 |
| rs774276322 | snp | C/T | 6.59391e-05 | 0.00574153 | intron-variant | CHAF1B | GRCh38.p7 | 21:36409370 | ACTGCAATTAATCCA[C/T]TAGGCCCATCGCTCA | 8208 |
| rs774367943 | in-del | -/AT | | | downstream-variant-500B | CHAF1B | GRCh38.p7 | 21:36417282 | ACATATATATGATAC[-/AT]ATATATATATATACA | 8208 |
| rs774375568 | in-del | -/AC | | | downstream-variant-500B | CHAF1B | GRCh38.p7 | 21:36417297 | TATATATATATATAC[-/AC]ACACACACACAAGTA | 8208 |
| rs774421311 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36388221 | TGGTAGAGTCAGGGA[A/G]GGAGGACAGCAAGAT | 8208 |
| rs774421360 | in-del | -/GCTGGAGTGCA | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36399082 | CGCTCTGTTGCCCAG[-/GCTGGAGTGCA]GTGCCACAATCTCAG | 8208 |
| rs774442214 | in-del | -/CCTCCCGGGCTCAAGTGAT | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36390743 | TCACTGCAGCCTCCA[-/CCTCCCGGGCTCAAGTGAT]CCTCCCACCTCAGCC | 8208 |
| rs774490978 | snp | A/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36392868 | AGGCAGGCGGCTGGG[A/T]GGTGGAGGTTGTAGC | 8208 |
| rs774577444 | in-del | -/TTTCTTTTTTTTTTT | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36382535 | CTATTTTTCTTTTTC[-/TTTCTTTTTTTTTTT]TTTTTTTTCAGACTG | 8208 |
| rs774604801 | snp | G/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36398731 | TCTGAAAAGAAGTCT[G/T]GTTGTCGTGTTTACT | 8208 |
| rs774679537 | snp | C/G | 1.66932e-05 | 0.002889 | missense | CHAF1B | GRCh38.p7 | 21:36413164 | CCAACAGTCATCAGG[C/G]ACCCTCCCTCCATCA | 8208 |
| rs774708665 | in-del | -/T | | | upstream-variant-2KB, intron-variant | CHAF1B | GRCh38.p7 | 21:36383967 | TTCTTTAGTCCAACA[-/T]TTGTGGTGCAAACTT | 8208 |
| rs774837946 | in-del | -/C | 9.44742e-05 | 0.00687228 | utr-variant-3-prime | CHAF1B | GRCh38.p7 | 21:36416372 | GGACCCTTGATGGGA[-/C]CTCGGCTTCTGCTCG | 8208 |
| rs774849385 | snp | A/T | 1.65255e-05 | 0.00287445 | intron-variant | CHAF1B | GRCh38.p7 | 21:36399644 | TTTCAGCAGCGCTTT[A/T]ACTGAGACTTAGGAA | 8208 |
| rs774902181 | snp | A/C | 3.3674e-05 | 0.00410315 | missense | CHAF1B | GRCh38.p7 | 21:36413233 | GAGAAGACCCTGCAG[A/C]CCAGTAGTCAAAACA | 8208 |
| rs774908427 | snp | A/G | 1.64735e-05 | 0.00286993 | synonymous-codon | CHAF1B | GRCh38.p7 | 21:36399557 | ACAGAAGAAGCGTGT[A/G]GCTTTCAATGTTTCG | 8208 |
| rs774923120 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36414954 | TACCTGTGTTTCGAC[A/G]CTTTCTATATATAGA | 8208 |
| rs774926872 | snp | A/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36395446 | TCCCATATGCTATGG[A/T]TTGTCAGAGGGTAAG | 8208 |
| rs774952968 | snp | A/G | | | intron-variant, upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36380497 | CCCAGGCTGGTCTCA[A/G]GAACTTCTGGGCTCA | 8208 |
| rs774965609 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36407481 | AGTTAACTTTCATGA[A/G]TAGTTGATTGAAACA | 8208 |
| rs774978522 | snp | A/G | 1.64765e-05 | 0.00287019 | synonymous-codon | CHAF1B | GRCh38.p7 | 21:36399527 | TTTCTTCAGGGTGCT[A/G]CGAGTATACAGTATA | 8208 |
| rs774978754 | snp | C/T | 1.67301e-05 | 0.00289219 | utr-variant-3-prime | MORC3 | GRCh38.p7 | 21:36375308 | TTAAAGTATATGTTA[C/T]GTAAGATAAAATATT | 8208 |
| rs775185246 | snp | G/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36387400 | TAATTTTTTAAATTT[G/T]CTGTAGAGACTAGGT | 8208 |
| rs775264268 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36402917 | CTGCTCCCGTTTTAC[A/G]CTGCAGCTTATCAGC | 8208 |
| rs775322217 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36410648 | TTCTGTGCCTCTCCA[C/T]GCTCCATTTTTCCTC | 8208 |
| rs775417400 | snp | A/T | 5.09117e-05 | 0.00504512 | missense | CHAF1B | GRCh38.p7 | 21:36413253 | TAGTCAAAACACAAA[A/T]GCCCACCCATCCCGG | 8208 |
| rs775439270 | snp | C/T | 4.94809e-05 | 0.00497373 | synonymous-codon, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36391603 | GGAGCCGGAGCAGAT[C/T]GCTTTTCAGGATGAG | 8208 |
| rs775456402 | snp | A/G | 1.6486e-05 | 0.00287102 | intron-variant | CHAF1B | GRCh38.p7 | 21:36391695 | GGGACCATGGCAGTG[A/G]TCTCTGTTTACGATG | 8208 |
| rs775503108 | snp | C/T | | | upstream-variant-2KB, intron-variant | CHAF1B | GRCh38.p7 | 21:36384863 | CGACTGATTTACAGC[C/T]TCACTTTAAAATGTT | 8208 |
| rs775549423 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36398639 | TGCTGGGATTACAGG[C/T]GTGAGCCACCTCGCC | 8208 |
| rs775554192 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36400527 | ATGGATGCCTTGGCC[C/T]CAACCTGAGTGGCGT | 8208 |
| rs775621829 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36415854 | ACCTCCCACGTTCAA[A/G]CAATTCTCCTGCCTC | 8208 |
| rs775657879 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36411760 | TTGAGACCAAGTATC[A/G]CTCTGTCACCCGGGC | 8208 |
| rs775713429 | snp | C/T | 7.40837e-05 | 0.00608575 | intron-variant | CHAF1B | GRCh38.p7 | 21:36413333 | AAGAACTTGTTGGAA[C/T]AAGATGTCATTGCAA | 8208 |
| rs775965583 | in-del | -/T | 1.65266e-05 | 0.00287455 | intron-variant | CHAF1B | GRCh38.p7 | 21:36411432 | GCCTTGTTTCTGTGG[-/T]TTTTACTTTGTCTCT | 8208 |
| rs775994347 | in-del | -/TTCTTTTTTTTTTT | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36382536 | TATTTTTCTTTTTCT[-/TTCTTTTTTTTTTT]TTTTTTTTCAGACTG | 8208 |
| rs776014948 | snp | A/G | 1.64827e-05 | 0.00287073 | missense, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36386161 | ATCACTTGTGAAATA[A/G]CCTGGCACAACAAGG | 8208 |
| rs776028572 | snp | A/C | 0.000301841 | 0.0122813 | | | GRCh38.p7 | 21:36377483 | AACAACTGTTGTTTA[A/C]CAGAACAACGTGGGC | 8208 |
| rs776051577 | in-del | -/GTGT | 0.000134106 | 0.00818749 | intron-variant | CHAF1B | GRCh38.p7 | 21:36397392 | ATGCTGTTTTGGTGC[-/GTGT]GTGTGTGTTTTTTTT | 8208 |
| rs776116430 | snp | A/C | | | upstream-variant-2KB, intron-variant | CHAF1B | GRCh38.p7 | 21:36383807 | GCGCCCGCCGCCACG[A/C]CCGACTAATTTTTTG | 8208 |
| rs776179627 | snp | C/T | | | intron-variant, upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36380391 | CCTTGGTGGGAATCT[C/T]TCTCAAAATGTGATA | 8208 |
| rs776195178 | snp | A/G | 1.6543e-05 | 0.00287597 | intron-variant | CHAF1B | GRCh38.p7 | 21:36387556 | GACAGTATAATATGT[A/G]CCCATTCTATGTTTT | 8208 |
| rs776230418 | snp | A/G | 1.65181e-05 | 0.00287381 | intron-variant | CHAF1B | GRCh38.p7 | 21:36399637 | CATTCTTTTTCAGCA[A/G]CGCTTTAACTGAGAC | 8208 |
| rs776260915 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36414033 | CAGGAGGTGCAGAGT[C/T]GTTTCTTCCCTGCTT | 8208 |
| rs776269311 | in-del | -/AAAA | 1.67105e-05 | 0.0028905 | intron-variant | CHAF1B | GRCh38.p7 | 21:36402734 | AACAAAAAAAATAAT[-/AAAA]ATAAATTTTGTGTGC | 8208 |
| rs776305264 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36399963 | GTGGGCGGATCACTT[A/G]AGGTCAGGAGTTTGA | 8208 |
| rs776321140 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36409097 | TGACCTCAAGTGGTC[C/T]GCTTGCCTCGGCCTC | 8208 |
| rs776384538 | snp | A/G | 1.65217e-05 | 0.00287412 | intron-variant | CHAF1B | GRCh38.p7 | 21:36411437 | TGTTTCTGTGGTTTT[A/G]CTTTGTCTCTGTCCC | 8208 |
| rs776398032 | snp | C/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36414909 | CGAACCATCTTGCCC[C/G]GCCCAACGCTCTGGA | 8208 |
| rs776403393 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36382494 | GTCCCGTTGTTCTCA[A/G]TCTCCTGTATTGATT | 8208 |
| rs776517405 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36400881 | GTTACTGGCTTCACA[C/T]GGGGACATGGTGCAA | 8208 |
| rs776561332 | snp | A/G | 9.88419e-05 | 0.00702931 | missense | CHAF1B | GRCh38.p7 | 21:36402827 | CTGAGTTTCACTCCC[A/G]ACGGATCTTTGCTTC | 8208 |
| rs776564047 | snp | A/G | 1.64909e-05 | 0.00287144 | intron-variant | CHAF1B | GRCh38.p7 | 21:36391710 | ATCTCTGTTTACGAT[A/G]AGTGCATTAAATGGA | 8208 |
| rs776617536 | snp | A/G | 3.29739e-05 | 0.00406028 | missense, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36391629 | ATGAGGACGAGGCCC[A/G]GCTGAACAAGGAGAA | 8208 |
| rs776636299 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36410396 | CCCTTCTCTTATTCA[A/G]ATACTCCCATTACAC | 8208 |
| rs776653217 | snp | A/G | 1.65449e-05 | 0.00287614 | missense, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36386257 | GGCGTGGACACCAAT[A/G]TCAGGGTAAACTGGG | 8208 |
| rs776677978 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36400237 | GTAATCCTAGCACTT[C/T]GGGAGGCTGAGGCAG | 8208 |
| rs776732427 | snp | A/G | 3.73636e-05 | 0.00432208 | intron-variant | CHAF1B | GRCh38.p7 | 21:36413342 | TTGGAACAAGATGTC[A/G]TTGCAAAATGAAACA | 8208 |
| rs776858705 | snp | C/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36415621 | GCAGGAGATTGTCTA[C/G]CTCAGGTTTCTCCAC | 8208 |
| rs776860143 | in-del | -/AA | | | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36378344 | TCAAAAAGCTTAAGT[-/AA]CATTTCATCATAGGA | 8208 |
| rs776954213 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36383004 | GAGCCACTACGCCTG[A/G]CTTCTCCTAGTTTTC | 8208 |
| rs776964270 | snp | A/G | 3.2981e-05 | 0.00406071 | missense | CHAF1B | GRCh38.p7 | 21:36413057 | GAGGGTCTTCGCCAG[A/G]ACCCAGACCGGTAGA | 8208 |
| rs776991651 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36416158 | TTCCATTATATCAGT[A/G]TAGGATCTTGCCAGG | 8208 |
| rs777021305 | in-del | -/GT | 1.87933e-05 | 0.00306534 | intron-variant | CHAF1B | GRCh38.p7 | 21:36397387 | GGTAATGCTGTTTTG[-/GT]GTGCGTGTGTGTGTG | 8208 |
| rs777024464 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36384402 | CATGGGGCTGAGTAG[A/G]GCCAGGAATCTGTAC | 8208 |
| rs777040850 | snp | C/T | 3.31235e-05 | 0.00406948 | missense | CHAF1B | GRCh38.p7 | 21:36412919 | TGGCCATTTCTTCCA[C/T]GGACGGTTACTGCTC | 8208 |
| rs777079304 | in-del | -/A | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36396358 | CTCACCAAAAACCTC[-/A]AAAAAAAAAAAAAAA | 8208 |
| rs777079920 | snp | A/G | 4.9579e-05 | 0.00497866 | intron-variant | CHAF1B | GRCh38.p7 | 21:36387567 | ATGTGCCCATTCTAT[A/G]TTTTTCAAATGAATG | 8208 |
| rs777150559 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36408154 | TTCCAAGAGCAGCAG[C/T]GTATGATGGTCACTC | 8208 |
| rs777396815 | snp | A/G | 1.65751e-05 | 0.00287876 | missense | CHAF1B | GRCh38.p7 | 21:36413104 | AGAACCCAAGACCCC[A/G]GCAGCCCCGGCACGA | 8208 |
| rs777429158 | in-del | -/TT | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36397729 | TAAATCTTTTTTTTT[-/TT]TTTTTTTTTTAGACA | 8208 |
| rs777430234 | in-del | -/A | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36402722 | GTGTAGAAAACAAAC[-/A]AAAAAAATAATAAAA | 8208 |
| rs777455472 | snp | C/T | 1.64866e-05 | 0.00287106 | intron-variant | CHAF1B | GRCh38.p7 | 21:36402889 | TAAAGGAATGATGGC[C/T]GAGTGGGGATGTCTG | 8208 |
| rs777589750 | snp | A/G | 3.32995e-05 | 0.00408027 | missense, intron-variant | CHAF1B | GRCh38.p7 | 21:36397444 | ATTTTTAATGAACAT[A/G]AAAGTTATGTCCAAG | 8208 |
| rs777635024 | snp | C/T | 1.64727e-05 | 0.00286986 | missense, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36387688 | GCCGTCAATGTTGTG[C/T]GTTTTTCTCCAACTG | 8208 |
| rs777642815 | snp | A/G | 4.94417e-05 | 0.00497176 | missense | CHAF1B | GRCh38.p7 | 21:36413033 | AGAAAACCAAGAGTC[A/G]GACACATCGAGGGTC | 8208 |
| rs777668457 | in-del | -/A | 0.00177899 | 0.0297713 | intron-variant, upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36380330 | TAAGGTAATTTGAGT[-/A]TAGAATTTTTTCTGT | 8208 |
| rs777727510 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36396104 | CTCCCGGGTTCAACA[A/G]TTCTCCTGCCTCAGC | 8208 |
| rs777760827 | snp | C/T | 1.69352e-05 | 0.00290987 | intron-variant | CHAF1B | GRCh38.p7 | 21:36415441 | GTAGAGTATCTTTTC[C/T]TTTGTTCTTTTGGAA | 8208 |
| rs777843184 | snp | A/C | | | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36378448 | TGCCTGTAATCCCAG[A/C]ACTTTGGGAGGCCAA | 8208 |
| rs777907811 | snp | A/G | 0.000153548 | 0.00876074 | synonymous-codon | CHAF1B | GRCh38.p7 | 21:36416279 | TAATGTTGCAGAGAC[A/G]CCTGGAGACGCTCAG | 8208 |
| rs777910180 | snp | C/T | 3.303e-05 | 0.00406373 | intron-variant | CHAF1B | GRCh38.p7 | 21:36409498 | GGGGTGTGTTATGTT[C/T]TCTCTCCGAAACAGG | 8208 |
| rs777927310 | snp | C/G | | | upstream-variant-2KB, intron-variant | CHAF1B | GRCh38.p7 | 21:36383694 | CGCTCTCTCGCCCAG[C/G]CTGGAGTGCAGTGGC | 8208 |
| rs778005013 | snp | A/T | 0.000523423 | 0.016169 | | | GRCh38.p7 | 21:36377389 | TTGGAAGCACTTAGA[A/T]ACTTTTTGCTCTTTA | 8208 |
| rs778040000 | snp | A/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36408710 | CTGTTGGTGAACAGT[A/T]TGCTGAAACAGTGAC | 8208 |
| rs778137838 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36391234 | TTAGCTCAGAAGGCA[A/G]TTTGCCTACTTTCCC | 8208 |
| rs778139508 | snp | C/G | 1.64806e-05 | 0.00287054 | missense | CHAF1B | GRCh38.p7 | 21:36411468 | CAACCCCCAGGTGTG[C/G]AGCTGATGAGTCTGC | 8208 |
| rs778206184 | snp | A/C | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36412332 | CCACCTTTTGGTCCC[A/C]AATTCAGCCCCCGTG | 8208 |
| rs778361845 | snp | C/G | 5.0385e-05 | 0.00501896 | missense | CHAF1B | GRCh38.p7 | 21:36413227 | TCGGAGGAGAAGACC[C/G]TGCAGCCCAGTAGTC | 8208 |
| rs778456382 | in-del | -/T | | | intron-variant, upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36380773 | TTTTGTGGAGACAGA[-/T]TTTTTGACTTGTTGC | 8208 |
| rs778585931 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36394854 | CTCCTGCCTCAGTCT[C/T]CCAAGTAGCTGGGAC | 8208 |
| rs778616636 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36398428 | GCAGTGGTGCGATCT[C/T]GGCATACTGTAACCT | 8208 |
| rs778640428 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36407961 | CCAGCCTGGGTGACA[A/G]AGCAAGACTCCATCT | 8208 |
| rs778650359 | snp | A/G | 1.64738e-05 | 0.00286995 | missense | CHAF1B | GRCh38.p7 | 21:36399590 | GATGCTGTCTGGAAT[A/G]GGGGCTGAAGGAGAG | 8208 |
| rs778656976 | in-del | -/A | 0.000115746 | 0.00760653 | intron-variant | CHAF1B | GRCh38.p7 | 21:36399648 | GCAGCGCTTTAACTG[-/A]AGACTTAGGAAGTCA | 8208 |
| rs778678313 | in-del | -/CTTT | | | intron-variant, upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36381110 | CTTTTTCTTCTTCTT[-/CTTT]TTTTTTTTTTTTTTT | 8208 |
| rs778748692 | in-del | -/AT | 5.02054e-05 | 0.00501001 | | | GRCh38.p7 | 21:36386308 | ACACTGCTTGAAGCA[-/AT]AGTTTTCATTCTTTT | 8208 |
| rs778775999 | snp | C/T | 0.000273598 | 0.0116929 | utr-variant-5-prime, upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36380294 | TCTTGGTTTGTACTG[C/T]GATCTGAACCATGAC | 8208 |
| rs778801653 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36406797 | AATCACCATGTTGTA[C/T]AAGAGATGGATCTTG | 8208 |
| rs778812835 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36399858 | TCAACCCTGGTTGCA[C/T]GGTGGAATCACCTGG | 8208 |
| rs778875793 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36397174 | CCCCGGTCCACATGT[A/G]TGATCCTTGCTTGTT | 8208 |
| rs778930055 | snp | C/T | 1.68069e-05 | 0.00289882 | stop-gained | CHAF1B | GRCh38.p7 | 21:36416292 | ACGCCTGGAGACGCT[C/T]AGGGCAGTCCCCCAG | 8208 |
| rs778935317 | snp | A/G | | | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36379589 | TAATATCTGATTGGC[A/G]TAGAGGAAAAAATAA | 8208 |
| rs778966887 | snp | A/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36408576 | AGGTAGAACTGGAGT[A/T]AGGGCTGAGAACAGA | 8208 |
| rs778973452 | in-del | -/TTA | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36382694 | CACCATGCCTGGCTG[-/TTA]TTATTATTATTATTA | 8208 |
| rs779054821 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36405833 | ATGGAAAGATATGTC[A/G]TGTTCTAACAATTAA | 8208 |
| rs779416080 | snp | A/G | 1.65941e-05 | 0.00288041 | missense | CHAF1B | GRCh38.p7 | 21:36415320 | TTAACACCCTTAAAG[A/G]CGGACACTCCACCAA | 8208 |
| rs779427056 | snp | A/G | 3.35661e-05 | 0.00409657 | synonymous-codon | CHAF1B | GRCh38.p7 | 21:36413214 | CTTGCCGGGGCCTTC[A/G]GAGGAGAAGACCCTG | 8208 |
| rs779485977 | snp | A/G | | | upstream-variant-2KB, intron-variant | CHAF1B | GRCh38.p7 | 21:36383502 | TTTATATCAATTTTC[A/G]TTATTAAAAAGTTCT | 8208 |
| rs779543059 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36398869 | AATAAAACAAATTGA[A/G]TATAAGATGGCCTTG | 8208 |
| rs779625542 | snp | A/G | 1.64768e-05 | 0.00287021 | synonymous-codon | CHAF1B | GRCh38.p7 | 21:36399605 | AGGGGCTGAAGGAGA[A/G]GTATAAAATATTTTG | 8208 |
| rs779644675 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36408401 | ATGAGGGTCCTAGGG[A/G]GAAAGGAGCCTGGGC | 8208 |
| rs779702547 | snp | C/T | 1.74644e-05 | 0.00295497 | synonymous-codon | CHAF1B | GRCh38.p7 | 21:36413287 | GTCACTCTGAACACA[C/T]TGCAAGCCTGGAGCA | 8208 |
| rs779727318 | snp | A/G | | | downstream-variant-500B | CHAF1B | GRCh38.p7 | 21:36417232 | ATGTGCCACCATGCC[A/G]TGCTAATTTCACACA | 8208 |
| rs779746864 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36414823 | TTGCCATGTTGGTCA[A/G]GCTGGTCGAAAACTC | 8208 |
| rs779803781 | snp | A/G | 1.64931e-05 | 0.00287163 | missense, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36386209 | GACTTCCAGCATGGG[A/G]CGGCTGGGAGGATCC | 8208 |
| rs779859359 | snp | G/T | 0.000137108 | 0.00827861 | intron-variant, upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36380333 | GGTAATTTGAGTATA[G/T]AATTTTTTCTGTTCT | 8208 |
| rs779933840 | snp | A/T | 1.66081e-05 | 0.00288163 | intron-variant | CHAF1B | GRCh38.p7 | 21:36402745 | TAATAAAAATAAATT[A/T]TGTGTGCGACAGGCA | 8208 |
| rs779982090 | snp | A/T | 1.95815e-05 | 0.00312896 | utr-variant-3-prime | CHAF1B | GRCh38.p7 | 21:36416379 | TGATGGGACCTCGGC[A/T]TCTGCTCGAAGCCTA | 8208 |
| rs780072017 | snp | A/G/T | 4.94184e-05 | 0.00497063 | missense | CHAF1B | GRCh38.p7 | 21:36411516 | GCTGTGGCCTCGGAG[A/G/T]ATTCCGTGCTTCTGT | 8208 |
| rs780185922 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36413514 | CCAGTTTCTGCCTGT[C/T]AGATAAAGCCCAGGC | 8208 |
| rs780287680 | snp | A/T | 6.62548e-05 | 0.00575526 | missense | MORC3 | GRCh38.p7 | 21:36375209 | TGTGCCTGATCTTGA[A/T]CTTCAGCAAGTGAAT | 8208 |
| rs780304260 | snp | A/G | 0.00011612 | 0.00761882 | synonymous-codon | CHAF1B | GRCh38.p7 | 21:36415322 | AACACCCTTAAAGAC[A/G]GACACTCCACCAAGT | 8208 |
| rs780358574 | snp | A/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36400572 | GAGGTAAGCAGGGCC[A/T]CCATGATTCTCAGGT | 8208 |
| rs780362779 | snp | A/C | | | | | GRCh38.p7 | 21:36377656 | GGCAAAATCAGTGAA[A/C]GCTGAGTGAGCACAC | 8208 |
| rs780462007 | snp | A/G | 3.31175e-05 | 0.00406911 | intron-variant | CHAF1B | GRCh38.p7 | 21:36415405 | GTAAGTAATATTGTT[A/G]CTGGTTTAATATAAT | 8208 |
| rs780522023 | snp | A/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36399724 | GCCGATTCCAGAACT[A/T]CAATAAGGCTTCCTT | 8208 |
| rs780524941 | snp | G/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36409771 | CCAAAATGCTGGGAT[G/T]ACAGGTGTGAGCCCC | 8208 |
| rs780539459 | snp | A/G | 1.64993e-05 | 0.00287218 | synonymous-codon | CHAF1B | GRCh38.p7 | 21:36402763 | TGTGCGACAGGCAAG[A/G]AGCTACCGGATGTTT | 8208 |
| rs780543285 | in-del | -/T | 0.0296962 | 0.118179 | intron-variant | CHAF1B | GRCh38.p7 | 21:36415749 | TTGCCCATGACATTC[-/T]TTTTTTTTTTTTCTT | 8208 |
| rs780552265 | snp | A/G | 4.96652e-05 | 0.00498298 | intron-variant | CHAF1B | GRCh38.p7 | 21:36408858 | GGAAATGTTTGAAAT[A/G]TTTACATTTTTTTTA | 8208 |
| rs780574961 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36388115 | GGCGTGAGCCACTGC[A/G]CCCGGCCTGGATATG | 8208 |
| rs780711316 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36395116 | AGTGCAATGTCACAA[C/T]CTTAGCTCACTGAAA | 8208 |
| rs780764051 | snp | C/G | 1.65015e-05 | 0.00287237 | missense, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36386223 | GACGGCTGGGAGGAT[C/G]CACAGACTGGCGTCT | 8208 |
| rs780776778 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36386674 | CAGAATGCTAAATTT[C/T]CAGGGCCTGCGGTGA | 8208 |
| rs780871054 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36408337 | AAGTTGGGGAAAGGC[A/G]AGTCTCAGCCTTTGG | 8208 |
| rs780876001 | snp | A/C | 3.54101e-05 | 0.00420759 | missense | CHAF1B | GRCh38.p7 | 21:36413302 | CTGCAAGCCTGGAGC[A/C]AGACAACACCCCGGT | 8208 |
| rs780937851 | snp | A/G | 1.64757e-05 | 0.00287012 | missense | CHAF1B | GRCh38.p7 | 21:36413014 | AGAACTCCTGATACA[A/G]CAAAGAAAACCAAGA | 8208 |
| rs781044532 | snp | C/T | 1.66167e-05 | 0.00288237 | intron-variant | CHAF1B | GRCh38.p7 | 21:36386287 | GGCAGAGATAGACAT[C/T]CGGGAACACTGCTTG | 8208 |
| rs781179903 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36397073 | AATACCTTCTTCCAC[C/T]CTTCATCCCCTCTTC | 8208 |
| rs781221859 | snp | C/G | 1.64882e-05 | 0.00287121 | missense, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36394603 | ATGGGAATTTAATGG[C/G]TTCTGCCTCTGTGGA | 8208 |
| rs781370344 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36398542 | TTTTTGTATTTTTAG[C/T]AGAGACAGAGTTTCA | 8208 |
| rs781384380 | snp | A/T | 0.000131796 | 0.00811668 | intron-variant | CHAF1B | GRCh38.p7 | 21:36387754 | TGCTGTCCTTCAGAG[A/T]TTCTTCGGGAACCAG | 8208 |
| rs781385270 | snp | A/G | | | | | GRCh38.p7 | 21:36377563 | GTATTGCTTCAACTA[A/G]TGTTTATTACTTTAA | 8208 |
| rs781421427 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36386473 | GCGGGACGTGGCAGT[A/G]TGCAGCTGTAGGCCC | 8208 |
| rs781456490 | snp | A/G | 1.6855e-05 | 0.00290297 | missense, intron-variant | CHAF1B | GRCh38.p7 | 21:36397423 | TTTGTAGGACAAAAG[A/G]TATCAATTTTTAATG | 8208 |
| rs781508485 | snp | A/G | 3.29989e-05 | 0.00406182 | intron-variant | CHAF1B | GRCh38.p7 | 21:36409484 | TCCTCAGAGCCTCAG[A/G]GGTGTGTTATGTTTT | 8208 |
| rs781548365 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36404940 | GTAGAGATGGGGTTT[C/T]GCCATGTTGGCCAGG | 8208 |
| rs781548594 | snp | A/C | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36390180 | CTCTACTAAAAATAC[A/C]AAATTAGCTGGGTGT | 8208 |
| rs781555740 | snp | C/T | 3.4626e-05 | 0.00416075 | intron-variant | CHAF1B | GRCh38.p7 | 21:36416272 | TGTTTGTTAATGTTG[C/T]AGAGACGCCTGGAGA | 8208 |
| rs781569310 | in-del | -/TTCTTTT | | | intron-variant, upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36381108 | TTCTTTTTCTTCTTC[-/TTCTTTT]TTTTTTTTTTTTTTT | 8208 |
| rs781645283 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36412455 | ACCTCCGCCTCCTGG[A/G]TTCAAGCAATTCTCC | 8208 |
| rs781753785 | snp | C/T | 4.96241e-05 | 0.00498092 | intron-variant | CHAF1B | GRCh38.p7 | 21:36391544 | CTGTTACTGAATCAC[C/T]CTGCAGATGCTGTCA | 8208 |
| rs796369838 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36398923 | TAGTGTTTATTTTTC[A/G]TAGAATCTTCTGTTG | 8208 |
| rs796527627 | in-del | -/AAAG | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36390334 | TGAAACACCATCTCA[-/AAAG]AAAAAAAAAAAAAAA | 8208 |
| rs796806735 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36394266 | TATTTTAGTAGAGAC[A/G]TGGTTTCACCATGTT | 8208 |