SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs8596 | snp | A/G | 0.34526 | 0.23114 | utr-variant-3-prime | CHAF1B | GRCh38.p7 | 21:36416582 | CATGAACGTTTTAAC[A/G]TAGTAAATCCTCTTT | 8208 |
rs9108 | snp | C/T | 0.00478085 | 0.0486577 | utr-variant-3-prime | MORC3 | GRCh38.p7 | 21:36376454 | CGTGTCGGTCATATA[C/T]AGTATTGAATTTTTA | 8208 |
rs170144 | snp | A/G | 0.498754 | 0.0249289 | intron-variant | CHAF1B | GRCh38.p7 | 21:36407192 | gcctcaggctcttga[A/G]tagctgggattacag | 8208 |
rs190068 | snp | C/T | 0.0490535 | 0.14873 | intron-variant | CHAF1B | GRCh38.p7 | 21:36410628 | gaggcacagaatata[C/T]aaggaaaacccaaag | 8208 |
rs218623 | snp | C/T | 0.250168 | 0.25 | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36378958 | GAAAATTAAAATGGC[C/T]AATGTAAGGACTGAG | 8208 |
rs218624 | snp | C/T | 0.250168 | 0.25 | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36379076 | GTGTCTGGGTAGTTT[C/T]TGGGTGGTGTGTGGC | 8208 |
rs218625 | snp | C/T | 0.250168 | 0.25 | intron-variant, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36381472 | AAAGAGACTATATTA[C/T]AGTCTCTTTTAGTTC | 8208 |
rs218626 | snp | C/T | 0.434398 | 0.168811 | intron-variant, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36381734 | tatcatattgggctc[C/T]gattttctggagaac | 8208 |
rs218627 | snp | A/G | 0.493793 | 0.055364 | upstream-variant-2KB, intron-variant | CHAF1B | GRCh38.p7 | 21:36383737 | GGCGTGAACCCGGGA[A/G]GCGGGGCTTGCAGTG | 8208 |
rs218628 | snp | C/T | 0.29278 | 0.246313 | intron-variant | CHAF1B | GRCh38.p7 | 21:36391054 | AACAGCAAAGAACCC[C/T]CAGTGCAAGGGTTGG | 8208 |
rs218629 | snp | G/T | 0.322959 | 0.239117 | intron-variant | CHAF1B | GRCh38.p7 | 21:36410045 | acctgggaggcaggg[G/T]ttgcagtgagccaag | 8208 |
rs218630 | snp | C/T | 0.481473 | 0.0944461 | intron-variant | CHAF1B | GRCh38.p7 | 21:36411772 | CACTGCACTCCAGCC[C/T]GGGTGACAGAGTGAT | 8208 |
rs218631 | snp | A/G | 0.427575 | 0.175975 | intron-variant | CHAF1B | GRCh38.p7 | 21:36413706 | CACCAAGAGGAAGAG[A/G]TGTCCAGGGCTTCCC | 8208 |
rs218646 | snp | C/T | 0.0733688 | 0.176922 | intron-variant | CHAF1B | GRCh38.p7 | 21:36402090 | AAAACAACATTTCTT[C/T]AACACCTGTCTGGGA | 8208 |
rs218647 | snp | G/T | 0.0170251 | 0.090679 | intron-variant | CHAF1B | GRCh38.p7 | 21:36403359 | AGCGATTCTCCTGCC[G/T]CAGTCTCCCAAGTGG | 8208 |
rs218648 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36404653 | tgaggtccggagttc[A/G]agaccagactgacca | 8208 |
rs218649 | snp | A/G | 0.49089 | 0.0668743 | intron-variant | CHAF1B | GRCh38.p7 | 21:36406388 | tgaggcagaagaatc[A/G]cttgaactcaggaga | 8208 |
rs218650 | snp | G/T | 0.493107 | 0.0583 | intron-variant | CHAF1B | GRCh38.p7 | 21:36406532 | ttgggaggctgaggc[G/T]ggtggatcacctgag | 8208 |
rs218651 | snp | A/G | 0.481009 | 0.0955756 | intron-variant | CHAF1B | GRCh38.p7 | 21:36407850 | GCCGGGATTACAGGC[A/G]CCTGCCACGATGCCC | 8208 |
rs218652 | snp | A/G | 0.490782 | 0.0672626 | intron-variant | CHAF1B | GRCh38.p7 | 21:36408524 | GTGGGCAATCCCCGG[A/G]GACCTGGTTCTGATC | 8208 |
rs968599 | snp | A/G | 0 | 0 | upstream-variant-2KB, intron-variant | CHAF1B | GRCh38.p7 | 21:36383462 | TCTTAACTCAGCTTC[A/G]AAAAAAAACTTCTCA | 8208 |
rs1063308 | snp | A/G | 0.0514469 | 0.15191 | utr-variant-3-prime | MORC3 | GRCh38.p7 | 21:36375309 | TAAAGTATATGTTAT[A/G]TAAGATAAAATATTT | 8208 |
rs1906483 | snp | A/G | 0.495056 | 0.049474 | intron-variant | CHAF1B | GRCh38.p7 | 21:36396833 | ATGACAAAGAGGGTC[A/G]CTAGTTAGGAGGTGA | 8208 |
rs1906484 | snp | C/G | 0.141258 | 0.225111 | intron-variant | CHAF1B | GRCh38.p7 | 21:36396825 | GAGGGTCACTAGTTA[C/G]GAGGTGACCGAGTAG | 8208 |
rs1906485 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | CHAF1B | GRCh38.p7 | 21:36396664 | TTCCttttttttttt[C/T]ttttttttttgagac | 8208 |
rs1906486 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | CHAF1B | GRCh38.p7 | 21:36396663 | TCCtttttttttttc[C/T]tttttttttgagaca | 8208 |
rs1906487 | snp | A/G | 0.0588605 | 0.161139 | intron-variant | CHAF1B | GRCh38.p7 | 21:36396603 | gcagtggcgccgtca[A/G]agctcactgcagcct | 8208 |
rs2129798 | snp | A/G | | | downstream-variant-500B | CHAF1B | GRCh38.p7 | 21:36417118 | cgccactgcactcca[A/G]cctgggcaacagagc | 8208 |
rs2269187 | snp | A/G | 0.496778 | 0.0400063 | intron-variant | CHAF1B | GRCh38.p7 | 21:36389066 | GGGGTAAGATCCCGC[A/G]TCGGTACCCAGCTTG | 8208 |
rs2633325 | snp | A/T | 0.00477324 | 0.0486193 | utr-variant-3-prime | MORC3 | GRCh38.p7 | 21:36376317 | AAAATATGGTTCTAA[A/T]ATATACATAGTTTAT | 8208 |
rs2835341 | snp | G/T | 0.495016 | 0.0496707 | intron-variant | CHAF1B | GRCh38.p7 | 21:36393837 | ATCTCATTTTAATGC[G/T]TAGTTCTGGAGATTG | 8208 |
rs2835342 | snp | G/T | 0.124491 | 0.216211 | intron-variant | CHAF1B | GRCh38.p7 | 21:36414379 | CATAATATGTGTATG[G/T]GTTGCTGGCTTTAAC | 8208 |
rs2845757 | snp | A/G | 0.280256 | 0.248162 | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36378492 | tgaggtcaggagatc[A/G]agaccatcctggcca | 8208 |
rs2850081 | snp | C/T | 0.440599 | 0.161778 | | | GRCh38.p7 | 21:36377391 | GGAAGCACTTAGATA[C/T]TTTTTGCTCTTTATG | 8208 |
rs3787734 | snp | A/G | 0.0335098 | 0.125028 | intron-variant | CHAF1B | GRCh38.p7 | 21:36414068 | CAGTGTGGCTGGCAC[A/G]CACGCCTGTGTCTGC | 8208 |
rs7275524 | snp | A/G | 0.137867 | 0.223442 | downstream-variant-500B | CHAF1B | GRCh38.p7 | 21:36417197 | ccacctcagcttccc[A/G]agtagctgggactac | 8208 |
rs7278517 | snp | C/T | 0.0501905 | 0.150254 | | | GRCh38.p7 | 21:36377274 | CCTTTTGGCCAGCTT[C/T]TCTATGTATTCTTGC | 8208 |
rs7278581 | snp | A/T | 0 | 0 | intron-variant | CHAF1B | GRCh38.p7 | 21:36399433 | TGAAAACTGTTGCGG[A/T]GGTAATAGGCTGTTG | 8208 |
rs7278593 | snp | A/G | 0.00953873 | 0.0683987 | downstream-variant-500B | MORC3 | GRCh38.p7 | 21:36377111 | caagagcgaaactcc[A/G]tctcaaaaaaaaaGG | 8208 |
rs7279180 | snp | C/T | 0.127944 | 0.218179 | intron-variant | CHAF1B | GRCh38.p7 | 21:36407080 | GCCAAGGTGGGTGGA[C/T]CACCTGAGGTCTGGA | 8208 |
rs7281977 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36398640 | gctgggattacaggc[A/G]tgagccacctcgccc | 8208 |
rs7282109 | snp | C/G | 0.495016 | 0.0496707 | intron-variant | CHAF1B | GRCh38.p7 | 21:36398712 | ATAAACTATTTTTGT[C/G]CTTTCTGAAAAGAAG | 8208 |
rs7282284 | snp | A/G | 0.00140614 | 0.0264782 | | | GRCh38.p7 | 21:36377431 | AAGTATTGCCAAGAT[A/G]TGAGACTTCGAAAAT | 8208 |
rs7509895 | snp | A/G | | | upstream-variant-2KB, intron-variant | CHAF1B | GRCh38.p7 | 21:36383806 | ggcgcccgccgccac[A/G]cccgactaatttttt | 8208 |
rs8126861 | snp | A/G | 0.168135 | 0.236216 | intron-variant | CHAF1B | GRCh38.p7 | 21:36388546 | ATCTTGGCTCACTGC[A/G]ACCTCTGCCTCCCAG | 8208 |
rs8127277 | snp | C/T | 0.216048 | 0.247684 | intron-variant | CHAF1B | GRCh38.p7 | 21:36394100 | tttttttttttgaga[C/T]ggagtctcactctgt | 8208 |
rs8127381 | snp | A/T | 0.495016 | 0.0496707 | intron-variant | CHAF1B | GRCh38.p7 | 21:36396182 | tttttgtatttttag[A/T]agagatggggtttgc | 8208 |
rs8127711 | snp | A/G | 0.0505692 | 0.150756 | intron-variant | CHAF1B | GRCh38.p7 | 21:36396112 | ttcaacaattctcct[A/G]cctcagccctcaagg | 8208 |
rs8127746 | snp | A/G | 0.0588605 | 0.161139 | intron-variant | CHAF1B | GRCh38.p7 | 21:36396202 | atggggtttgcccat[A/G]ttggccaggctggtc | 8208 |
rs8128974 | snp | C/G | 0.0505692 | 0.150756 | intron-variant | CHAF1B | GRCh38.p7 | 21:36392402 | attcgacaaaaccgc[C/G]atcgtcatcatggcc | 8208 |
rs8129103 | snp | C/T | 0.0599851 | 0.162463 | intron-variant | CHAF1B | GRCh38.p7 | 21:36392460 | tcccagacggggtgg[C/T]ggccgggtagagggg | 8208 |
rs8129295 | snp | C/T | 0.216349 | 0.247725 | intron-variant | CHAF1B | GRCh38.p7 | 21:36390666 | gatatattgttatcc[C/T]catttttgagacagg | 8208 |
rs8129487 | snp | A/G | 0.0596104 | 0.162024 | intron-variant | CHAF1B | GRCh38.p7 | 21:36392526 | cgccccccacctccc[A/G]gacggggcagctggc | 8208 |
rs8129667 | snp | A/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36401337 | tttaatatgttatat[A/T]tttatattatatata | 8208 |
rs8130019 | snp | G/T | 0.00279162 | 0.0372561 | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36378488 | atcatgaggtcagga[G/T]atcgagaccatcctg | 8208 |
rs8130294 | snp | C/T | 0.0588605 | 0.161139 | intron-variant | CHAF1B | GRCh38.p7 | 21:36392593 | gctgccgggcagaga[C/T]gctcctctcttccca | 8208 |
rs8132242 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36382620 | tcttggctcactgcc[C/T]tctgggttcaagtga | 8208 |
rs8133286 | snp | C/G | 0 | 0 | intron-variant | CHAF1B | GRCh38.p7 | 21:36398879 | ATTGAATATAAGATG[C/G]CCTTGGAATAAAAGT | 8208 |
rs9754126 | snp | A/G | 0.274736 | 0.248773 | intron-variant | CHAF1B | GRCh38.p7 | 21:36389761 | AGTGCATGAAGGGAT[A/G]TGTGTGTGTGTGTGT | 8208 |
rs9754297 | snp | A/G | | | downstream-variant-500B | MORC3 | GRCh38.p7 | 21:36376755 | GCAGTTTATTTTTTG[A/G]AGACTGTTTCCATTA | 8208 |
rs9754317 | snp | G/T | | | downstream-variant-500B | MORC3 | GRCh38.p7 | 21:36376754 | TGCAGTTTATTTTTT[G/T]AAGACTGTTTCCATT | 8208 |
rs9978761 | snp | A/G | 0.5 | 0 | intron-variant | CHAF1B | GRCh38.p7 | 21:36404879 | ctcctgagtagctga[A/G]attacaggcgcctgc | 8208 |
rs10483033 | snp | A/G | 0.0693013 | 0.172766 | intron-variant | CHAF1B | GRCh38.p7 | 21:36405327 | tatataaaaattcct[A/G]tctttcgtctatatt | 8208 |
rs10529380 | in-del | -/T | 0 | 0 | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36379904 | TTTTTTTTTTTTTTT[-/T]GAAACAAAGTATCAT | 8208 |
rs11088346 | snp | A/G | 0.067446 | 0.170804 | intron-variant | CHAF1B | GRCh38.p7 | 21:36403551 | TATGGAAGCCATAGC[A/G]CTAAAGCCAAAGATA | 8208 |
rs11280868 | in-del | -/GCAACCTCC | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36382616 | TGATCTTGGCTCACT[-/GCAACCTCC]GCCCTCTGGGTTCAA | 8208 |
rs11701086 | snp | C/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36386562 | acgatcactccactg[C/G]actccagcctgggtg | 8208 |
rs11701134 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36386748 | agacggagtcttgct[C/T]tgttgcccaggtggg | 8208 |
rs12151974 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36382560 | tttttttttttttca[A/G]actgagtctgtttct | 8208 |
rs12627489 | snp | A/G | 0.330482 | 0.236691 | intron-variant | CHAF1B | GRCh38.p7 | 21:36394207 | tcaccctcctgagta[A/G]ctgggtctgcaggtg | 8208 |
rs13046055 | snp | A/C | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36407214 | gcctgaggcaggaga[A/C]tcgctccaacccagg | 8208 |
rs13046137 | snp | G/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36407071 | ctctgggaggccaag[G/T]tgggtggatcacctg | 8208 |
rs13046178 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CHAF1B | GRCh38.p7 | 21:36407256 | gcagtgagccaagat[C/T]gcaccactgcactct | 8208 |
rs13046248 | snp | C/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36407156 | aaaatacaaaaatta[C/G]ccgggcatggtgatg | 8208 |
rs13046340 | snp | C/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36407257 | cagtgagccaagatc[C/G]caccactgcactcta | 8208 |
rs13046392 | snp | G/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36392865 | ccaaggcaggcggct[G/T]ggaggtggaggttgt | 8208 |
rs13046430 | snp | C/G | 0.326741 | 0.23793 | intron-variant | CHAF1B | GRCh38.p7 | 21:36400292 | TGGGACTGGCCTGGC[C/G]AACATGGTGAAACCC | 8208 |
rs13046747 | snp | G/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36407072 | tctgggaggccaagg[G/T]gggtggatcacctga | 8208 |
rs13047955 | snp | G/T | | | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36379134 | ATCCACAGTAGGTTG[G/T]Ctttttttttttttt | 8208 |
rs13048698 | snp | C/G | 0.497829 | 0.0328757 | intron-variant | CHAF1B | GRCh38.p7 | 21:36389988 | CAGGGCCAATGGCAT[C/G]TTAACCAAGCTCCCA | 8208 |
rs13049605 | snp | C/T | 0.327211 | 0.237778 | intron-variant | CHAF1B | GRCh38.p7 | 21:36400540 | CCCCAACCTGAGTGG[C/T]GTGATTCACTTGGCT | 8208 |
rs13050414 | snp | C/T | 0.366473 | 0.221211 | intron-variant | CHAF1B | GRCh38.p7 | 21:36399288 | TGATTCACCCGCCTC[C/T]GCCTCCCAAAGTGTC | 8208 |
rs13051031 | snp | G/T | 0.011928 | 0.0763002 | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36379865 | ATTTGGCTGTAGTTC[G/T]TTTTTTTTTtttttt | 8208 |
rs13053082 | snp | A/C | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36407115 | aagaccagcctggcc[A/C]acatggcaaaaccct | 8208 |
rs13053094 | snp | A/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36407146 | gtctctactaaaaat[A/T]caaaaattagccggg | 8208 |
rs16994052 | snp | C/G | 0.00835141 | 0.0640778 | utr-variant-3-prime | MORC3 | GRCh38.p7 | 21:36375674 | TATTTTTCTCTAAGT[C/G]GAGGGCTATGCCATA | 8208 |
rs16994069 | snp | G/T | 0.0696718 | 0.173152 | downstream-variant-500B | CHAF1B | GRCh38.p7 | 21:36417024 | TTCATATGCAATTTG[G/T]TATCTAAATAGGTTA | 8208 |
rs28361428 | snp | A/G | 0.5 | 0 | intron-variant | CHAF1B | GRCh38.p7 | 21:36391972 | TGGGTGTTTCTCGGA[A/G]AGGGGGATTTGGCAG | 8208 |
rs28576459 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36392106 | TCCCTGGGTACTTGA[A/G]ATTAGGGAGTGGTGA | 8208 |
rs28691871 | snp | A/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36405276 | TAGTATTAGAATTTT[A/T]AAAATAATTTGATAA | 8208 |
rs34332851 | in-del | -/C | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36409296 | TGAGCCACCGCGCCC[-/C]TGCCAAAATGTTTAC | 8208 |
rs34390263 | in-del | -/A | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36411779 | GTCACCCAGGCTGGA[-/A]GTGCAGTGGTGTGAT | 8208 |
rs34476947 | in-del | -/C | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36415690 | TGTGGAGGACTGTCC[-/C]TGTGTATTATGCGAT | 8208 |
rs34638024 | in-del | -/T | 0 | 0 | intron-variant | CHAF1B | GRCh38.p7 | 21:36382557 | TTTTTTTTTTTTTTT[-/T]CAGACTGAGTCTGTT | 8208 |
rs34926522 | in-del | -/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36388488 | TTTTTTTTTTTTTTT[-/T]GAGACAGTCTCACTG | 8208 |
rs35051347 | in-del | -/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36402914 | TGTCTGCTCCCGTTT[-/T]ACGCTGCAGCTTATC | 8208 |
rs35343767 | in-del | -/C | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36415721 | TTTAACAGCATCCCC[-/C]GGCTGCTACTTCTTG | 8208 |
rs35488336 | in-del | -/T | 0.359998 | 0.2245 | intron-variant | CHAF1B | GRCh38.p7 | 21:36411117 | TTCTTATAAATATTC[-/T]TTTTTTTTTTTTTTG | 8208 |
rs35580662 | in-del | -/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36410418 | CCATTACACATGTAT[-/T]ATATTAGGTCCTTTG | 8208 |
rs35604187 | in-del | -/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36398250 | GTAAAGATGGGATTT[-/T]GCCATGTTGCCCAGG | 8208 |
rs35630362 | in-del | -/G | 0.334871 | 0.235153 | intron-variant | CHAF1B | GRCh38.p7 | 21:36394429 | AGCCAGGCTGGCCTT[-/G]GAACTCCTGACCACA | 8208 |
rs35658312 | in-del | -/T | | | utr-variant-3-prime | MORC3 | GRCh38.p7 | 21:36376159 | ATACTACATACCTTT[-/T]ATTATATTACAAACC | 8208 |
rs35705526 | snp | C/T | 0.330714 | 0.236612 | intron-variant | CHAF1B | GRCh38.p7 | 21:36402978 | CGACTTACCTGCCCA[C/T]TGGAACCTCCAGGAG | 8208 |
rs36078668 | in-del | -/T | 0.453575 | 0.145111 | intron-variant, upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36381288 | ACCATGCCTGGCTGA[-/T]TTTTTTTTTTTTTTT | 8208 |
rs36087741 | in-del | -/C | | | | | GRCh38.p7 | 21:36377755 | GTTGGTGACGCTGCC[-/C]TGTGATCTCAGACGC | 8208 |
rs36094135 | in-del | -/T | 0.0178098 | 0.0926698 | intron-variant | CHAF1B | GRCh38.p7 | 21:36397293 | TACAGAGTCTCTCAC[-/T]TACTGCCTGCTGAGT | 8208 |
rs55655429 | snp | C/G | 0.494976 | 0.0498674 | intron-variant | CHAF1B | GRCh38.p7 | 21:36393990 | CTGCAATCTCTGCCT[C/G]CTGGGTTCAGGGGAT | 8208 |
rs55895669 | snp | A/G | 0.495016 | 0.0496707 | intron-variant | CHAF1B | GRCh38.p7 | 21:36389830 | ATTTGTAGAGGGAAA[A/G]GTGGGGAGCAGGAGC | 8208 |
rs55920360 | in-del | -/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36391937 | TTTTTTTTTTTTTTT[-/T]AGTATTTATTGATCA | 8208 |
rs56118104 | snp | C/T | | | synonymous-codon, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36391664 | ACGGTTGTGAAGACT[C/T]TGCGGTAACTTGGGA | 8208 |
rs56187769 | snp | G/T | 0.0379877 | 0.132479 | intron-variant | CHAF1B | GRCh38.p7 | 21:36400700 | TTACTATCTTGGCAG[G/T]TAGGTAGAGAGTTTT | 8208 |
rs56281312 | snp | G/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36387224 | AATAAGCATAGTTTT[G/T]TTTTTTTTTTTTTTT | 8208 |
rs56382962 | snp | A/T | 0.16846 | 0.236329 | intron-variant | CHAF1B | GRCh38.p7 | 21:36393912 | CTTTTTGTTTTGTTT[A/T]GTTTAGAGTCAGAGT | 8208 |
rs56714492 | in-del | -/A | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36407317 | AAAAAAAAAAAAAAA[-/A]GTATATGTTCAAGGA | 8208 |
rs57197480 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | CHAF1B | GRCh38.p7 | 21:36412485 | CTGCCTCAGCCTCCC[C/G]AATAGCTGGGATTAC | 8208 |
rs57596540 | in-del | -/CTAAAGTTTTTTTTTGC | 0.334182 | 0.235401 | intron-variant | CHAF1B | GRCh38.p7 | 21:36389682 | AAATAAAACAGAAAT[-/CTAAAGTTTTTTTTTGC]AGGAGGAGGAAAAGA | 8208 |
rs58186613 | snp | C/T | 0.081446 | 0.184634 | intron-variant | CHAF1B | GRCh38.p7 | 21:36397929 | GACAGGGTTTCACCA[C/T]GTTGGTCAAGCTGTT | 8208 |
rs58672732 | in-del | -/TGAT | | | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36378300 | ATTATACCATATAAT[-/TGAT]AACTAAACATTTCCA | 8208 |
rs59270005 | snp | C/T | 0.104504 | 0.2033 | intron-variant | CHAF1B | GRCh38.p7 | 21:36399397 | CAGTTGTGAATATCA[C/T]TGGTAAAAGCTTTTG | 8208 |
rs59272936 | in-del | -/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36410688 | CTTTTTTTTTTTTTT[-/T]CTTGCTCTGTTGCCC | 8208 |
rs59317575 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36391749 | TTTGACTTTTTTTTT[C/T]TTTTCTTTTGAGATA | 8208 |
rs59627355 | snp | A/T | 0.32768 | 0.237625 | upstream-variant-2KB, intron-variant | CHAF1B | GRCh38.p7 | 21:36385172 | AATGGATAATAATAA[A/T]AAATAATAATGAATC | 8208 |
rs60389156 | in-del | -/TGCGCG | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36389801 | GTGTGTGTGTGTGTG[-/TGCGCG]CGCGCGCACGCTGAT | 8208 |
rs60572556 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | CHAF1B | GRCh38.p7 | 21:36404203 | CCTCCCAGTTTCAAG[C/T]GATTCTCCTGCCTCA | 8208 |
rs60992072 | snp | A/T | 0.31014 | 0.242659 | intron-variant | CHAF1B | GRCh38.p7 | 21:36391481 | AAAAAAAAAAAAAAA[A/T]GAAAATAAAAATCCT | 8208 |
rs61141750 | snp | A/G | | | upstream-variant-2KB, intron-variant | CHAF1B | GRCh38.p7 | 21:36384020 | TTTTTTTTTTTTTGA[A/G]AAAATATTTGACAGC | 8208 |
rs61308860 | snp | A/C | 0.497695 | 0.0338674 | intron-variant | CHAF1B | GRCh38.p7 | 21:36395887 | TTGTTGTTGGCTGCC[A/C]CCGCAGCACTGTGTC | 8208 |
rs61437805 | in-del | -/TT | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36387240 | TTTTTTTTTTTTTTT[-/TT]GAGACAGGGTCTTAC | 8208 |
rs61593376 | in-del | -/TTT | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36404757 | TTTTTTTTTTTTTTT[-/TTT]AAAAAGCAGAGTCTC | 8208 |
rs62229403 | snp | C/G | 0.175897 | 0.238765 | intron-variant | CHAF1B | GRCh38.p7 | 21:36383192 | GTCCCGGGTTCAATG[C/G]ATTCTCTTGCCTCAG | 8208 |
rs62229404 | snp | C/T | 0.128247 | 0.218349 | missense, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36387659 | TTTTGTCCAATCTTG[C/T]TCGTCATACCAAAGC | 8208 |
rs62229405 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | CHAF1B | GRCh38.p7 | 21:36389206 | AGGGAGCATACCGGG[A/G]GTGTCATTAATGAAT | 8208 |
rs62229406 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36394077 | CTATTTTTTTTTTGG[C/T]TAATTTTTTTTTTTT | 8208 |
rs62229407 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36394078 | TATTTTTTTTTTGGC[C/T]AATTTTTTTTTTTTT | 8208 |
rs62229409 | snp | A/G | 0.115788 | 0.21092 | intron-variant | CHAF1B | GRCh38.p7 | 21:36396330 | ATCATAAGTGTGATG[A/G]GTTGTTACTGAACCT | 8208 |
rs62229410 | snp | G/T | 0.0174175 | 0.0916809 | intron-variant | CHAF1B | GRCh38.p7 | 21:36405525 | GCCTTGATCTCCTGA[G/T]TTCAGGGAATCCTCC | 8208 |
rs62982361 | snp | A/C | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36396655 | CCACACCCTGTCTCA[A/C]AAAAAAAAGAAAAAA | 8208 |
rs66712452 | in-del | -/GCCCA | 0.494143 | 0.0537956 | intron-variant | CHAF1B | GRCh38.p7 | 21:36405043 | GGTGTGAGCCACTGC[-/GCCCA]GCCCCAGTAGCAAAT | 8208 |
rs67850591 | snp | A/G | 0.167484 | 0.23599 | intron-variant | CHAF1B | GRCh38.p7 | 21:36400958 | AGGCACTGAGAGGTC[A/G]CACCTGTGAAGTAAG | 8208 |
rs68081676 | snp | C/T | 0.167484 | 0.23599 | intron-variant | CHAF1B | GRCh38.p7 | 21:36400658 | GACAGGCAGGTCGAG[C/T]GTTGGATCTGTCTGG | 8208 |
rs71198806 | in-del | -/TTT | | | intron-variant, upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36381132 | TTTTTTTTTTTTTTT[-/TTT]CTTTTGCGACAGGTC | 8208 |
rs71198807 | in-del | -/T | 0.498133 | 0.030494 | intron-variant | CHAF1B | GRCh38.p7 | 21:36383088 | TTTTTTTTTTTTTTT[-/T]GAGACAGAATCTCAC | 8208 |
rs71198808 | in-del | -/G | 0 | 0 | intron-variant | CHAF1B | GRCh38.p7 | 21:36390337 | AACACCATCTCAAAA[-/G]AAAAAAAAAAAAAAG | 8208 |
rs71198809 | in-del | -/A | 0 | 0 | intron-variant | CHAF1B | GRCh38.p7 | 21:36403481 | AAAAAAAAAAAAAAA[-/A]GAAACTTTACTATTT | 8208 |
rs71319536 | in-del | AACCTCCGCCT/CC | 0.5 | 0 | intron-variant | CHAF1B | GRCh38.p7 | 21:36382620 | ATCTTGGCTCACTGC[AACCTCCGCCT/CC]TCTGGGTTCAAGTGA | 8208 |
rs71326682 | in-del | -/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | CHAF1B | GRCh38.p7 | 21:36384001 | TTTTTTTTTTTTTTT[-/T]GAGAAAATATTTGAC | 8208 |
rs71326683 | in-del | -/TT | 0.5 | 0 | intron-variant | CHAF1B | GRCh38.p7 | 21:36387225 | ATAAGCATAGTTTTG[-/TT]TTTTTTTTTTTTTTT | 8208 |
rs71326686 | in-del | -/A | 0.5 | 0 | intron-variant | CHAF1B | GRCh38.p7 | 21:36403455 | AGTGATATCTTATCT[-/A]AAAAAAAAAAAAAAA | 8208 |
rs71330675 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36380071 | TTTGAATATTTTGTA[A/G]AGACTGGGTTTGCCA | 8208 |
rs71330676 | snp | C/T | 0.335559 | 0.234904 | intron-variant | CHAF1B | GRCh38.p7 | 21:36388694 | CTGGTCTCAAACTCC[C/T]GAGCTCAGGCAATCT | 8208 |
rs71330677 | snp | C/T | 0.5 | 0 | intron-variant | CHAF1B | GRCh38.p7 | 21:36393228 | AGAGGGAGAGGGAGA[C/T]GGTGGAGGGAGAGGG | 8208 |
rs71330678 | snp | A/T | 0.5 | 0 | intron-variant | CHAF1B | GRCh38.p7 | 21:36402734 | AACAAAAAAAATAAT[A/T]AAAATAAATTTTGTG | 8208 |
rs73383722 | snp | C/T | 0.158632 | 0.232706 | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36378735 | CCACACATGATTTTC[C/T]GATTAAATCCAGAGT | 8208 |
rs73383726 | snp | A/G | 0.0325976 | 0.123435 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | CHAF1B | GRCh38.p7 | 21:36384724 | CTGTGTGTTTCTTTT[A/G]TCCAGTAAAAGCAGC | 8208 |
rs73383788 | snp | C/T | 0.0547245 | 0.156101 | intron-variant | CHAF1B | GRCh38.p7 | 21:36391369 | TATTTTTAGTAGAGA[C/T]AGTTAGCCAGGATGG | 8208 |
rs73385704 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | CHAF1B | GRCh38.p7 | 21:36408677 | TTTTGCAAACCGGAC[C/G]TGAAGGCTCTTGAGT | 8208 |
rs73385706 | snp | G/T | 0.0213599 | 0.101112 | intron-variant | CHAF1B | GRCh38.p7 | 21:36411614 | TTCATGGTGAGTGGC[G/T]GCTAATGAGGGAGAG | 8208 |
rs73385709 | snp | C/G | 0.031825 | 0.122064 | intron-variant | CHAF1B | GRCh38.p7 | 21:36412342 | GTCCCCAATTCAGCC[C/G]CCGTGGCCTGCTTGG | 8208 |
rs73902503 | snp | A/G | 0.343924 | 0.231686 | intron-variant | CHAF1B | GRCh38.p7 | 21:36397279 | ACACAGGGTTTTAGT[A/G]CAGAGTCTCTCACTT | 8208 |
rs73902504 | snp | A/G | 0.167294 | 0.235932 | intron-variant | CHAF1B | GRCh38.p7 | 21:36397554 | AATTTCTTTGTATTT[A/G]CTTGGAATTTTCTGA | 8208 |
rs73902505 | snp | A/G | 0.126564 | 0.217402 | intron-variant | CHAF1B | GRCh38.p7 | 21:36399328 | GGCGTGAGCTACCGC[A/G]CCCGGCCTGTAATAT | 8208 |
rs73902506 | snp | C/T | 0.140581 | 0.224783 | intron-variant | CHAF1B | GRCh38.p7 | 21:36402506 | TACATATAGCTTTAC[C/T]TAACAAAAATGTGTG | 8208 |
rs73905811 | snp | C/T | 0.126219 | 0.217206 | intron-variant | CHAF1B | GRCh38.p7 | 21:36388762 | GTGAGCCACCGCGCC[C/T]GGGCTATTTGGGCAT | 8208 |
rs73905812 | snp | C/T | 0 | 0 | intron-variant | CHAF1B | GRCh38.p7 | 21:36389798 | GTGTGTGTGTGTGTG[C/T]GTGCGCGCGCACGCT | 8208 |
rs73905813 | snp | C/T | 0.375 | 0.216506 | intron-variant | CHAF1B | GRCh38.p7 | 21:36389800 | GTGTGTGTGTGTGTG[C/T]GCGCGCGCACGCTGA | 8208 |
rs74408204 | snp | A/G | 0.0227574 | 0.104215 | | | GRCh38.p7 | 21:36377471 | AGTTGCAGACAGAAC[A/G]ACTGTTGTTTAACAG | 8208 |
rs74408856 | snp | A/G | 0.0142736 | 0.0832652 | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36379713 | CCTTTTAAAGCCACA[A/G]TTTCTTAGAGAGTCA | 8208 |
rs74510795 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CHAF1B | GRCh38.p7 | 21:36407418 | GGTGAATGAATCTTG[C/T]AGTAAATATTATGCA | 8208 |
rs74683276 | snp | C/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36389334 | CAGGCTGGGCGCGGT[C/G]GCTCACACATGTTGT | 8208 |
rs74725232 | in-del | -/AGCCC | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36405047 | TGAGCCACTGCGCCC[-/AGCCC]CAGTAGCAAATCCTT | 8208 |
rs74900401 | snp | A/C | 0.0104528 | 0.071534 | missense | CHAF1B | GRCh38.p7 | 21:36415317 | AACTTAACACCCTTA[A/C]AGACGGACACTCCAC | 8208 |
rs74922437 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | CHAF1B | GRCh38.p7 | 21:36406112 | AAAAAGATCTCAGGA[C/T]ATAAGGCGATTTAAT | 8208 |
rs74932300 | snp | G/T | 0.5 | 0 | intron-variant | CHAF1B | GRCh38.p7 | 21:36387241 | TTTTTTTTTTTTTTT[G/T]AGACAGGGTCTTACT | 8208 |
rs75089106 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36413374 | AAAATGCAGACAGAA[A/C]GCTCCCACCCTGCTG | 8208 |
rs75369579 | snp | G/T | 0 | 0 | intron-variant | CHAF1B | GRCh38.p7 | 21:36398069 | TATTTTTTTTTTTTT[G/T]TGAGAGAGGGGCTTA | 8208 |
rs75466152 | in-del | -/TT | | | upstream-variant-2KB, intron-variant | CHAF1B | GRCh38.p7 | 21:36384016 | CTTTTTTTTTTTTTT[-/TT]GAGAAAATATTTGAC | 8208 |
rs75506239 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | CHAF1B | GRCh38.p7 | 21:36408580 | AGAACTGGAGTAAGG[A/G]CTGAGAACAGACAGT | 8208 |
rs75530000 | snp | C/T | 0.149586 | 0.228948 | intron-variant | CHAF1B | GRCh38.p7 | 21:36408748 | TCCTCTCCCTCCCTT[C/T]CCTGTTCCCCAGCTG | 8208 |
rs75727002 | snp | C/G/T | 0 | 0 | intron-variant | CHAF1B | GRCh38.p7 | 21:36394533 | CTTTTTTCCTCTTTG[C/G/T]TTTTGGATTCTAGGG | 8208 |
rs75728133 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CHAF1B | GRCh38.p7 | 21:36386914 | AGATGGGGTTTTACC[A/G]TGTTGGCCAGGCTGG | 8208 |
rs75765616 | snp | C/T | 0.0501905 | 0.150254 | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36379526 | ATAGAATCCTATCTG[C/T]ATATTTGTCTGTTGA | 8208 |
rs75799198 | snp | G/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | CHAF1B | GRCh38.p7 | 21:36384015 | ACTTTTTTTTTTTTT[G/T]TTGAGAAAATATTTG | 8208 |
rs75876284 | snp | A/G | 0.0588605 | 0.161139 | intron-variant | CHAF1B | GRCh38.p7 | 21:36399706 | AATCACTGGCCACAA[A/G]GAGCCGATTCCAGAA | 8208 |
rs75918925 | snp | C/T | 0.0209421 | 0.100162 | upstream-variant-2KB, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36384589 | CATGAGACACGGATT[C/T]GTAGGCAATTTCTGT | 8208 |
rs76204867 | snp | C/T | 0 | 0 | intron-variant | CHAF1B | GRCh38.p7 | 21:36410688 | TCTTTTTTTTTTTTT[C/T]CTTGCTCTGTTGCCC | 8208 |
rs76206539 | snp | C/G | 0.0577344 | 0.159793 | utr-variant-3-prime, downstream-variant-500B | MORC3 | GRCh38.p7 | 21:36376644 | CTAACTGTTCAAATG[C/G]TACTTTTAAAGACTT | 8208 |
rs76520089 | snp | C/T | 0 | 0 | intron-variant | CHAF1B | GRCh38.p7 | 21:36382557 | TTTTTTTTTTTTTTT[C/T]CAGACTGAGTCTGTT | 8208 |
rs76531747 | snp | A/G | 0.0588605 | 0.161139 | intron-variant | CHAF1B | GRCh38.p7 | 21:36389203 | GGGAGGGAGCATACC[A/G]GGAGTGTCATTAATG | 8208 |
rs76626926 | snp | A/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36382964 | CCGCCCGCTTCAGCC[A/T]CCCAGATGCTGCAAT | 8208 |
rs76752016 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | CHAF1B | GRCh38.p7 | 21:36413696 | CCCTTCTCTGGGGAA[A/G]CCCTGGACACCTCTT | 8208 |
rs76867470 | snp | A/C | 0.5 | 0 | intron-variant | CHAF1B | GRCh38.p7 | 21:36395375 | CTTTAAAAGCAACAC[A/C]AAAAATTGTTTTAGT | 8208 |
rs77011471 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHAF1B | GRCh38.p7 | 21:36396778 | CCCTGTTCGCATTGT[C/T]TGCTCTGGGCCCTCC | 8208 |
rs77020109 | snp | A/G | 0.0501905 | 0.150254 | intron-variant | CHAF1B | GRCh38.p7 | 21:36414034 | AGGAGGTGCAGAGTC[A/G]TTTCTTCCCTGCTTA | 8208 |
rs77027976 | snp | G/T | 0.0603597 | 0.1629 | upstream-variant-2KB, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36384758 | TCCAGAGGTACTTGT[G/T]TCCTGGCCTTCTGCG | 8208 |
rs77041804 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | CHAF1B | GRCh38.p7 | 21:36414231 | CCCTCTGCCTCCCAA[C/T]CTTCCCATAAACTGA | 8208 |
rs77117619 | snp | A/T | 0.0333695 | 0.124785 | intron-variant | CHAF1B | GRCh38.p7 | 21:36402459 | TAAGAGTTTTTAAAA[A/T]TAATTTTAGAACCAC | 8208 |
rs77219553 | snp | C/G | 0.5 | 0 | intron-variant | CHAF1B | GRCh38.p7 | 21:36388971 | CACTGTGGAAACCCC[C/G]GCAATGCTCCCTTTC | 8208 |
rs77584598 | snp | C/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36388607 | AAGTAGCTGGGATTA[C/G]AGGCGCCTGCCACCA | 8208 |
rs77601541 | snp | C/T | 0.0588605 | 0.161139 | intron-variant | CHAF1B | GRCh38.p7 | 21:36391076 | TTTGCTGTTTTGTTT[C/T]TCTATTCAGCTATTT | 8208 |
rs77784643 | snp | A/T | 0.0154538 | 0.0865337 | intron-variant | CHAF1B | GRCh38.p7 | 21:36398772 | CATTTAATTGTATTG[A/T]TGGAACAAAGAGTTA | 8208 |
rs78048870 | snp | A/G | 0.0588605 | 0.161139 | intron-variant | CHAF1B | GRCh38.p7 | 21:36388800 | AAACTGGGATATGAA[A/G]GAATTCAGCAATGGC | 8208 |
rs78092906 | snp | A/G | 0.0498117 | 0.149749 | intron-variant | CHAF1B | GRCh38.p7 | 21:36382522 | ATTTCCGTCATTTCT[A/G]TTTTTCTTTTTCTTT | 8208 |
rs78115313 | snp | A/T | 0.5 | 0 | intron-variant | CHAF1B | GRCh38.p7 | 21:36391479 | AAAAAAAAAAAAAAA[A/T]ATGAAAATAAAAATC | 8208 |
rs78147539 | snp | A/T | 0.139564 | 0.224285 | intron-variant | CHAF1B | GRCh38.p7 | 21:36414642 | TTTGAGACAGGGTCT[A/T]GCTCTGTTGCCCGGG | 8208 |
rs78289545 | snp | C/T | 0.000152712 | 0.00873685 | utr-variant-3-prime | MORC3 | GRCh38.p7 | 21:36375336 | ATTTGCTCAATTCTT[C/T]TGGTTGTACAGCTTT | 8208 |
rs78390596 | in-del | -/NTT | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36399050 | ATTTTTTTTTTTTTT[-/NTT]TTTTGAGACAGAATC | 8208 |
rs78397887 | snp | C/T | 0 | 0 | intron-variant | CHAF1B | GRCh38.p7 | 21:36410676 | CTCTTGCTGCTTTCT[C/T]TTTTTTTTTTTTCTT | 8208 |
rs78673386 | snp | A/G | 0.0588605 | 0.161139 | intron-variant | CHAF1B | GRCh38.p7 | 21:36397352 | GTCATAGTTTATACT[A/G]TTTGGGCTCAAACAG | 8208 |
rs78979512 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CHAF1B | GRCh38.p7 | 21:36415595 | TCCTGGTGAGCCAGG[C/G]AGTGGGTTCAGCAGG | 8208 |
rs79012123 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | CHAF1B | GRCh38.p7 | 21:36414220 | TCTCCACCAAGCCCT[C/T]TGCCTCCCAACCTTC | 8208 |
rs79092750 | snp | A/G | 0.342134 | 0.232404 | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36379572 | CACAAGATGAATGCT[A/G]TTAATATCTGATTGG | 8208 |
rs79110763 | snp | G/T | 0.0185938 | 0.0946107 | intron-variant, upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36380369 | ATTGTCTCTTGTTTT[G/T]TGACTCCCTTGGTGG | 8208 |
rs79169278 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | CHAF1B | GRCh38.p7 | 21:36413501 | TCTGTTTGTTCCTCC[A/G]GTTTCTGCCTGTCAG | 8208 |
rs79188563 | snp | A/G | 0.126219 | 0.217206 | intron-variant | CHAF1B | GRCh38.p7 | 21:36400348 | GCCGGGTGCATGCAT[A/G]TGATCCCAGCTATTC | 8208 |
rs79338835 | snp | C/G | 0.0498117 | 0.149749 | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36379256 | GGCCCAAATGCTCCA[C/G]CTGCCTCAGCCTCCC | 8208 |
rs79510506 | snp | A/G/T | 0.0154538 | 0.0865337 | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36379501 | TCACTGAAGTGGCTT[A/G/T]AAAATCTAAATAGAA | 8208 |
rs79681142 | snp | C/G | 0.0588605 | 0.161139 | intron-variant | CHAF1B | GRCh38.p7 | 21:36388250 | ATGAAACCAGGAACA[C/G]CTGTTTGAAAACAGC | 8208 |
rs79723935 | snp | A/C | 0.0146672 | 0.084371 | intron-variant | CHAF1B | GRCh38.p7 | 21:36400824 | TTTTTGTAAAGGAAT[A/C]AAGGCTACCGAGGCA | 8208 |
rs79729599 | snp | G/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36395103 | TTGTCCAGGTTGGAG[G/T]GCAATGTCACAATCT | 8208 |
rs79751129 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | CHAF1B | GRCh38.p7 | 21:36413685 | CCTCTGTCCTTCCCT[C/T]CTCTGGGGAAGCCCT | 8208 |
rs79832929 | snp | C/T | 0.5 | 0 | intron-variant | CHAF1B | GRCh38.p7 | 21:36403240 | AGGCGGGCGGATCAC[C/T]TGAGGTCAAGAGTTC | 8208 |
rs80082293 | snp | C/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36382966 | GCCCGCTTCAGCCTC[C/G]CAGATGCTGCAATTA | 8208 |
rs80088522 | snp | C/T | 0.00597247 | 0.0543191 | utr-variant-3-prime | MORC3 | GRCh38.p7 | 21:36375912 | TGAGATTGCCAATCA[C/T]GGTTAAACACAAAGT | 8208 |
rs80120755 | snp | C/T | 0.0146672 | 0.084371 | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36378966 | TTACATTGGCCATTT[C/T]AATTTTCTGTGTTTT | 8208 |
rs80125021 | in-del | -/AA/AACCTCCG | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36382618 | ATCTTGGCTCACTGC[-/AA/AACCTCCG]CCTCTGGGTTCAAGT | 8208 |
rs80151438 | snp | G/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | CHAF1B | GRCh38.p7 | 21:36384018 | TTTTTTTTTTTTTTT[G/T]AGAAAATATTTGACA | 8208 |
rs80203452 | snp | A/T | 0.0520825 | 0.152737 | intron-variant | CHAF1B | GRCh38.p7 | 21:36387393 | ACTTGGCTAATTTTT[A/T]AAATTTTCTGTAGAG | 8208 |
rs80252186 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36397780 | AGGCAGGTGTTGTGG[C/T]GCAATCTCACAATCT | 8208 |
rs111303661 | snp | C/T | 0.5 | 0 | intron-variant | CHAF1B | GRCh38.p7 | 21:36383297 | GAAGGGGTTTTGCCA[C/T]GTTGGCCAGGCTGGT | 8208 |
rs111450902 | snp | A/G | 0.5 | 0 | utr-variant-3-prime | MORC3 | GRCh38.p7 | 21:36375768 | TGTAGTAACACTCCT[A/G]ATACAACTCTGGTTA | 8208 |
rs111462996 | snp | A/G | 0.184521 | 0.241273 | intron-variant | CHAF1B | GRCh38.p7 | 21:36385523 | CCAGAGGCCCTCGCC[A/G]AGGGCGGGCCCCTGG | 8208 |
rs111622524 | snp | G/T | 0 | 0 | intron-variant | CHAF1B | GRCh38.p7 | 21:36387999 | AGTTTTTTTGTGTGT[G/T]TTTAGTAGAGACAGG | 8208 |
rs111722616 | snp | A/C | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 21:36377162 | TTTACTCTAGAGAAA[A/C]CTTGCCTAAATAATA | 8208 |
rs111782050 | snp | C/T | 0.0337553 | 0.125452 | intron-variant | CHAF1B | GRCh38.p7 | 21:36415022 | TGTTCACAAGACCGT[C/T]GGTAATGAACAGAAC | 8208 |
rs111786621 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CHAF1B | GRCh38.p7 | 21:36402686 | TGAGTGTAAAGATTT[A/G]GAAAAATGTTTAAGC | 8208 |
rs111821825 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36379473 | TTTTGTGCAGTGTCT[C/T]ATAAACAGGGACTCA | 8208 |
rs111856334 | snp | C/T | 0 | 0 | intron-variant, upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36381110 | CTTTTTCTTCTTCTT[C/T]TTTTTTTTTTTTTTT | 8208 |
rs111891883 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHAF1B | GRCh38.p7 | 21:36402298 | GCCTGGGTGACAGAG[C/T]GAGACTCTGTATCTA | 8208 |
rs112039579 | snp | A/T | 0.5 | 0 | intron-variant | CHAF1B | GRCh38.p7 | 21:36386384 | TCCCAGTGCTTTGGG[A/T]GGCTGAGGTGAGAGG | 8208 |
rs112147556 | in-del | -/CT | 0.5 | 0 | intron-variant | CHAF1B | GRCh38.p7 | 21:36411763 | AGACCAAGTATCACT[-/CT]GTCACCCGGGCTGGA | 8208 |
rs112174707 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | CHAF1B | GRCh38.p7 | 21:36414869 | CTGCCCGCCTCAGCC[C/T]GCCAAAGTGCTGGGA | 8208 |
rs112324894 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHAF1B | GRCh38.p7 | 21:36390225 | GTAGTCCCAGCTATT[C/T]GGGAGGCTGAGGCAG | 8208 |
rs112454319 | snp | A/G | 0.0162398 | 0.0886349 | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36379043 | GCTGTAAAGAAGCTG[A/G]AAGCTTGTGTTAATT | 8208 |
rs112517403 | in-del | -/T | 0.5 | 0 | intron-variant | CHAF1B | GRCh38.p7 | 21:36396003 | TCTTGTTTTGTGTGG[-/T]TTTTTTTTTTTATTT | 8208 |
rs112578378 | snp | A/G | 0.101658 | 0.201233 | intron-variant | CHAF1B | GRCh38.p7 | 21:36400457 | GCCTGGGTGACAAGA[A/G]CGAAACTCAGTCTCA | 8208 |
rs112615523 | snp | C/G | 0.187369 | 0.242028 | intron-variant | CHAF1B | GRCh38.p7 | 21:36392967 | GCAATCCCGGCACCT[C/G]GGGAGGCTGAGGCTG | 8208 |
rs112681426 | snp | C/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36407864 | GTGCCTGTAATCCCG[C/G]CTACTCAGGAGGCTG | 8208 |
rs112749984 | snp | C/T | 0.5 | 0 | intron-variant | CHAF1B | GRCh38.p7 | 21:36383152 | GGAGTGCAGTGGTGC[C/T]ATCTCAGCTCACTGC | 8208 |
rs112877857 | snp | C/T | 0.5 | 0 | intron-variant | CHAF1B | GRCh38.p7 | 21:36387311 | CAGTGCAGCCCCGAC[C/T]CGGGGCTCAAGTGAT | 8208 |
rs113087996 | snp | C/T | 0.5 | 0 | intron-variant | CHAF1B | GRCh38.p7 | 21:36401634 | TATTTTTATATTATA[C/T]ATAATATATATTTTT | 8208 |
rs113112731 | in-del | -/GT | 0.5 | 0 | intron-variant | CHAF1B | GRCh38.p7 | 21:36411132 | TTTTTTTTTTTTTTT[-/GT]GACAGAGTCTTCCTC | 8208 |
rs113116661 | snp | C/T | 0.141934 | 0.225437 | intron-variant | CHAF1B | GRCh38.p7 | 21:36392733 | ACCTCCCAGACAGGG[C/T]GGCGGGGCAGAGGCG | 8208 |
rs113194466 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36416215 | TATTCTGTAAATGTC[A/G]GCCCTTGACTTCCAG | 8208 |
rs113206316 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CHAF1B | GRCh38.p7 | 21:36390503 | AGTTATTGGACTTAG[A/G]CAATGGGTGACCTCA | 8208 |
rs113227084 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | CHAF1B | GRCh38.p7 | 21:36414899 | ATTACAGGTGCGAAC[C/T]ATCTTGCCCGGCCCA | 8208 |
rs113265788 | snp | C/G | 0.5 | 0 | intron-variant | CHAF1B | GRCh38.p7 | 21:36404904 | GCCTGCCACCACAAC[C/G]AGATAATTTTTGTAT | 8208 |
rs113332086 | snp | C/G | 0.5 | 0 | downstream-variant-500B | CHAF1B | GRCh38.p7 | 21:36416879 | TTATTCTTTTAGTAA[C/G]TAAGTGAAGTGAAAA | 8208 |
rs113341085 | in-del | -/T | 0.5 | 0 | intron-variant | CHAF1B | GRCh38.p7 | 21:36410674 | CCTCTTGCTGCTTTC[-/T]TTTTTTTTTTTTTTC | 8208 |
rs113382620 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | CHAF1B | GRCh38.p7 | 21:36402619 | TCAACAATAAATGAC[A/G]CTATGTAAAGAAAAC | 8208 |
rs113382956 | snp | C/T | 0.344815 | 0.231323 | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36378531 | AAACCCCATCTCTAC[C/T]AAAAATACAAAAATT | 8208 |
rs113388736 | snp | A/G | 0.00302656 | 0.038783 | synonymous-codon | CHAF1B | GRCh38.p7 | 21:36411494 | TCTGCCCTACCGCCT[A/G]GTGTTTGCTGTGGCC | 8208 |
rs113471028 | snp | G/T | 0.139903 | 0.224452 | intron-variant | CHAF1B | GRCh38.p7 | 21:36410198 | GAACTCCTGACCTCA[G/T]GTGATCCACCCACCT | 8208 |
rs113542793 | snp | C/T | 0.5 | 0 | utr-variant-3-prime | CHAF1B | GRCh38.p7 | 21:36416547 | TGCTGTTGTATTCAG[C/T]ATCCATTTTTAACTT | 8208 |
rs113683232 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | CHAF1B | GRCh38.p7 | 21:36399848 | ACAGTGGTTTTCAAC[C/G]CTGGTTGCACGGTGG | 8208 |
rs113707310 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | CHAF1B | GRCh38.p7 | 21:36393646 | TTTAGTAGAGACGGG[G/T]TTTCTCCATGTTGGT | 8208 |
rs113737251 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | CHAF1B | GRCh38.p7 | 21:36382998 | AGGCGTGAGCCACTA[C/T]GCCTGGCTTCTCCTA | 8208 |
rs114016800 | snp | A/G | 0.0189856 | 0.0955633 | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36378764 | GTGTAAATTGTTAAC[A/G]GTGAATATTGATAGG | 8208 |
rs114018584 | snp | C/T | 0.00524511 | 0.0509416 | synonymous-codon | CHAF1B | GRCh38.p7 | 21:36413259 | AAACACAAAAGCCCA[C/T]CCATCCCGGAGGGTC | 8208 |
rs114109249 | snp | C/T | 0.0588605 | 0.161139 | intron-variant | CHAF1B | GRCh38.p7 | 21:36393853 | TAGTTCTGGAGATTG[C/T]CCTTATATTTTTGAT | 8208 |
rs114311378 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | CHAF1B | GRCh38.p7 | 21:36390039 | ATTCCGGTTAACTTA[A/G]CATGGGAATGCAGGC | 8208 |
rs114386479 | snp | C/T | 0.000494136 | 0.0157106 | synonymous-codon | CHAF1B | GRCh38.p7 | 21:36402802 | CAGCATGAAGTCTTT[C/T]TTCCGTAGACTGAGT | 8208 |
rs114421448 | snp | A/G | 0.0562307 | 0.157967 | intron-variant | CHAF1B | GRCh38.p7 | 21:36405929 | TTTGTTTAGTAGAAT[A/G]AATGCTGAAGAATAG | 8208 |
rs114514257 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | CHAF1B | GRCh38.p7 | 21:36409836 | GGAGCAAAGACTGGG[A/G]TTATCAAAATACATG | 8208 |
rs114524458 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | CHAF1B | GRCh38.p7 | 21:36414050 | TTTCTTCCCTGCTTA[C/T]ATCAGTGTGGCTGGC | 8208 |
rs114560300 | snp | A/T | 0.030278 | 0.119257 | upstream-variant-2KB, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36384519 | TATCCGGATTATGTT[A/T]TTCTAGCTTCCTGTA | 8208 |
rs114867967 | snp | A/C | 0.0154538 | 0.0865337 | intron-variant | CHAF1B | GRCh38.p7 | 21:36391495 | ATGAAAATAAAAATC[A/C]TAATATGAAGGAGTG | 8208 |
rs114918192 | snp | A/G | 0.0588605 | 0.161139 | intron-variant | CHAF1B | GRCh38.p7 | 21:36389513 | CAGGAGGCTGAGGTG[A/G]AGAATCGCTGTAACC | 8208 |
rs115050809 | snp | A/C/T | 0.00327825 | 0.0403537 | missense | CHAF1B | GRCh38.p7 | 21:36413066 | CGCCAGGACCCAGAC[A/C/T]GGTAGAGGGAACCCC | 8208 |
rs115097161 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | CHAF1B | GRCh38.p7 | 21:36386677 | AATGCTAAATTTCCA[A/G]GGCCTGCGGTGAACA | 8208 |
rs115117611 | snp | C/T | 0.0170251 | 0.090679 | downstream-variant-500B | CHAF1B | GRCh38.p7 | 21:36416979 | ATTTTTGTGGATCTA[C/T]TTATTCTAAAAAGAG | 8208 |
rs115158427 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | CHAF1B | GRCh38.p7 | 21:36402102 | GTTAAAGAAATGTTG[C/T]TTTAAAAGATTAATG | 8208 |
rs115392153 | snp | A/C/T | 0.00724059 | 0.0597324 | missense | CHAF1B | GRCh38.p7 | 21:36415321 | TAACACCCTTAAAGA[A/C/T]GGACACTCCACCAAG | 8208 |
rs115394807 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | CHAF1B | GRCh38.p7 | 21:36400866 | GCGGGGAGCAAGCTG[A/G]TTACTGGCTTCACAC | 8208 |
rs115409047 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36416045 | AGGCGTGAGCCACCG[C/T]GCCCAGCTTGCCCAT | 8208 |
rs115413133 | snp | C/G | 0.0592355 | 0.161582 | upstream-variant-2KB, intron-variant | CHAF1B | GRCh38.p7 | 21:36383621 | TGAGGAATCTAGTTA[C/G]AATTGCGTTATAGGA | 8208 |
rs115636196 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | CHAF1B | GRCh38.p7 | 21:36387010 | TGAGCCACCATGCCC[A/G]GCTCTGCTTTCTTAT | 8208 |
rs115769027 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | CHAF1B | GRCh38.p7 | 21:36394479 | CCTCCCAAAGTGCTG[A/G]GATTACAGGGGTAAG | 8208 |
rs115785460 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | CHAF1B | GRCh38.p7 | 21:36397135 | TCTTCTCAGACCCTC[C/T]GCCCTGTGCTGTCAG | 8208 |
rs115887891 | snp | G/T | 0.0588605 | 0.161139 | intron-variant | CHAF1B | GRCh38.p7 | 21:36388448 | TTTAGGACTGTGTTA[G/T]TAATTAATTGGCTTT | 8208 |
rs116006149 | snp | C/T | 0.0260105 | 0.111035 | utr-variant-3-prime | MORC3 | GRCh38.p7 | 21:36375765 | TAATGTAGTAACACT[C/T]CTGATACAACTCTGG | 8208 |
rs116174460 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | CHAF1B | GRCh38.p7 | 21:36414470 | TTTGTTTTTATGTGA[C/T]GGAAGGTATTCCTTG | 8208 |
rs116661943 | snp | C/T | 0.0456336 | 0.143994 | intron-variant | CHAF1B | GRCh38.p7 | 21:36410729 | GCAGTGGTATAATCT[C/T]GGCTCGTTGCAGCCT | 8208 |
rs116807863 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36381399 | AAATGTTGATATTAC[C/T]GGCATAAGCCACTGT | 8208 |
rs116846998 | snp | C/T | 0.00173773 | 0.0294253 | synonymous-codon | MORC3 | GRCh38.p7 | 21:36375227 | TCAGCAAGTGAATTA[C/T]GATGTTGATGTAGTT | 8208 |
rs116937506 | snp | A/G | 0.0337553 | 0.125452 | intron-variant | CHAF1B | GRCh38.p7 | 21:36405113 | TTAAAATCAAGTAGC[A/G]AATGGATGTCTGTTA | 8208 |
rs116995016 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | CHAF1B | GRCh38.p7 | 21:36397391 | AATGCTGTTTTGGTG[C/T]GTGTGTGTGTGTTTT | 8208 |
rs117217082 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CHAF1B | GRCh38.p7 | 21:36414801 | CATTTTTAGTAGAGA[C/T]GAGGTTTTGCCATGT | 8208 |
rs117284714 | snp | C/G | 0.0341408 | 0.126114 | intron-variant | CHAF1B | GRCh38.p7 | 21:36403289 | ATGGTGAAACACCCT[C/G]TCTATTAAAAATACA | 8208 |
rs117385888 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | CHAF1B | GRCh38.p7 | 21:36397589 | AGGTATTTATCGTAA[C/G]TTAGCCAAGATTTAT | 8208 |
rs117389851 | snp | A/G | 0.0452528 | 0.143452 | intron-variant | CHAF1B | GRCh38.p7 | 21:36383166 | CCATCTCAGCTCACT[A/G]CAACCTCCAAGTCCC | 8208 |
rs117466993 | snp | C/T | 0.0475351 | 0.146656 | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36378850 | GCAGGAATTTATACT[C/T]AGGATGAGTAATAAA | 8208 |
rs117676008 | snp | C/G | 0.0337553 | 0.125452 | intron-variant, upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36380831 | CAAGCGATGCACTCC[C/G]CCACCTCTTAACCTC | 8208 |
rs117676932 | snp | C/T | 0.0588605 | 0.161139 | intron-variant | CHAF1B | GRCh38.p7 | 21:36389408 | GTCAGGAGTTTGAGA[C/T]CAGCCTGGCCAATAT | 8208 |
rs117705655 | snp | C/T | 0.211819 | 0.247067 | downstream-variant-500B | MORC3 | GRCh38.p7 | 21:36376841 | TTTTTCTCAGCCTGG[C/T]GCAGTGGCTCACGCC | 8208 |
rs117756678 | snp | C/T | 0.030665 | 0.119967 | intron-variant | CHAF1B | GRCh38.p7 | 21:36409793 | GTGAGCCCCTGTGCC[C/T]GGCCTGGTTTAGTTA | 8208 |
rs117773195 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | CHAF1B | GRCh38.p7 | 21:36412426 | GTGCAGTGGAACGAT[C/T]GTGGCTCACTACAAC | 8208 |
rs117773599 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | CHAF1B | GRCh38.p7 | 21:36393253 | AGAGGGAGAGGGAGA[A/G]GATTTTTAAATTTCT | 8208 |
rs117809388 | snp | A/G | 0.0341408 | 0.126114 | intron-variant | CHAF1B | GRCh38.p7 | 21:36385873 | TCTGGATGTAGCGGC[A/G]TATCATAAACTTGTG | 8208 |
rs117885228 | snp | C/T | 0.212122 | 0.247114 | intron-variant, upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36381235 | AAGTGCTTCGCCTTC[C/T]TCAGCCTCCCAAGTA | 8208 |
rs117935346 | snp | C/T | 0.0498117 | 0.149749 | intron-variant | CHAF1B | GRCh38.p7 | 21:36382271 | GATTACCTTTTCTCC[C/T]GTGGGTGGACATTTG | 8208 |
rs118011319 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 21:36377749 | AGGTCCAGTTGGTGA[C/T]GCTGCCTGTGATCTC | 8208 |
rs118053617 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | CHAF1B | GRCh38.p7 | 21:36391778 | TAGGGTCTCATTGTC[A/G]CCCAGGCTGGAGTGC | 8208 |
rs138082504 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | CHAF1B | GRCh38.p7 | 21:36389571 | GATTGGGCCATTGCA[C/T]TCCAGCCTGGGCAAC | 8208 |
rs138120217 | snp | A/C | 0.000184575 | 0.00960485 | synonymous-codon | CHAF1B | GRCh38.p7 | 21:36416297 | TGGAGACGCTCAGGG[A/C]AGTCCCCCAGAGCTA | 8208 |
rs138148812 | snp | C/G | 0.328382 | 0.237395 | intron-variant | CHAF1B | GRCh38.p7 | 21:36392308 | agaacaaaatggagt[C/G]tcctatgtctacctc | 8208 |
rs138149380 | in-del | -/AGTT | | | upstream-variant-2KB, intron-variant | CHAF1B | GRCh38.p7 | 21:36383477 | CGAAGCTGAGTTAAG[-/AGTT]AGTCCCTTTATATCA | 8208 |
rs138222670 | snp | C/T | 0.0588605 | 0.161139 | intron-variant | CHAF1B | GRCh38.p7 | 21:36386801 | TTACTGCAACCTCTG[C/T]CTCCCAGGTTCAAGC | 8208 |
rs138313100 | snp | A/C | | | utr-variant-3-prime | MORC3 | GRCh38.p7 | 21:36376116 | CTACAGGTTAATGTG[A/C]GTTGAGGAAGACAGT | 8208 |
rs138341387 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36401153 | ATGCCTGTAGTCCCA[A/G]CTACTCCGGTGGCTG | 8208 |
rs138353793 | snp | A/G | 0.0479149 | 0.147179 | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36379321 | CCAGCTAATTTTTCT[A/G]TTTTTTGTAGAGATG | 8208 |
rs138448124 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CHAF1B | GRCh38.p7 | 21:36405766 | AGGGGCAGGACCTTT[A/G]TGGAGAAGTCTAGAA | 8208 |
rs138584664 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | CHAF1B | GRCh38.p7 | 21:36393309 | CCCAGGCTGGTCTAA[G/T]TTAGAAGTTTTATTT | 8208 |
rs138611384 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CHAF1B | GRCh38.p7 | 21:36396989 | TCTGTACCCATTAGC[A/G]GTTCTCAGCTACCTC | 8208 |
rs138792816 | snp | C/T | 0.118235 | 0.212457 | intron-variant | CHAF1B | GRCh38.p7 | 21:36404503 | GCAATGGCACGATCT[C/T]GGCTCACAGCAACCT | 8208 |
rs138801558 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36384377 | CGGGCCTCTGCTGGA[G/T]ATTCGGAATCATGGG | 8208 |
rs138860000 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHAF1B | GRCh38.p7 | 21:36410722 | CTGGGGTGCAGTGGT[A/G]TAATCTCGGCTCGTT | 8208 |
rs138871427 | snp | A/C | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36397784 | AGGTGTTGTGGCGCA[A/C]TCTCACAATCTCAGC | 8208 |
rs138882376 | snp | C/T | 8.23974e-05 | 0.00641809 | synonymous-codon | CHAF1B | GRCh38.p7 | 21:36402781 | CTACCGGATGTTTCA[C/T]GACGACAGCATGAAG | 8208 |
rs138894470 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CHAF1B | GRCh38.p7 | 21:36413796 | GGCCCTTCAGCCTTT[C/T]CCTTGTCACCACACA | 8208 |
rs138923185 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36389987 | TCAGGGCCAATGGCA[C/T]GTTAACCAAGCTCCC | 8208 |
rs138990766 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | CHAF1B | GRCh38.p7 | 21:36401996 | TCCGCCCGCCTTGGC[C/T]TCCCAAAGTGCTGGG | 8208 |
rs139087148 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | CHAF1B | GRCh38.p7 | 21:36387848 | TTTGAGATAGAGTTT[C/T]ACTCTTGTTCCCCAG | 8208 |
rs139122203 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | CHAF1B | GRCh38.p7 | 21:36399216 | ATTTTTTGTATTTTT[A/G]GTAGAGATGGGGTTT | 8208 |
rs139229934 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CHAF1B | GRCh38.p7 | 21:36394137 | GCTGGAGTGTAGTGG[C/T]GCGATCTTGGCTCAC | 8208 |
rs139345406 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36406188 | TTTGTAATTAATTGT[A/C]TGTTACTTAAATAAT | 8208 |
rs139378813 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36409694 | GTAGCGACAGCGTTT[C/T]ACCATGTTGCCAAGG | 8208 |
rs139434920 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | CHAF1B | GRCh38.p7 | 21:36411361 | TCAAGTGATCCACCC[A/G]GCTCGGCCTCCCAAA | 8208 |
rs139573855 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | CHAF1B | GRCh38.p7 | 21:36415493 | GTCAGTTCTGAGACA[A/G]CAGGGATGCATCTTA | 8208 |
rs139594054 | snp | A/C | 0.000153988 | 0.00877328 | missense | CHAF1B | GRCh38.p7 | 21:36412995 | GAAGCCAGTTTTGAA[A/C]ATGAGAACTCCTGAT | 8208 |
rs139617441 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | CHAF1B | GRCh38.p7 | 21:36415147 | ATTAAACAAGTGGGC[A/G]CATCTTACTATTTAA | 8208 |
rs139646018 | snp | A/G | | | | | GRCh38.p7 | 21:36377442 | AGATATGAGACTTCG[A/G]AAATGTGGCTCACAG | 8208 |
rs139656847 | snp | C/T | 0.158302 | 0.232576 | intron-variant | CHAF1B | GRCh38.p7 | 21:36390287 | GTGGTGAGCCAAGAT[C/T]GCACCATTGCACTCC | 8208 |
rs139759947 | snp | A/T | | | intron-variant, upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36380631 | TGTCACCCAGGCTCG[A/T]GTAGCAGTGGCGCGA | 8208 |
rs139892744 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36407359 | AGCATTGTTTATAGT[A/G]GTAAAAAACCAAAAG | 8208 |
rs139980774 | snp | C/T | 0.00200793 | 0.0316217 | synonymous-codon | CHAF1B | GRCh38.p7 | 21:36402829 | GAGTTTCACTCCCGA[C/T]GGATCTTTGCTTCTC | 8208 |
rs140258736 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CHAF1B | GRCh38.p7 | 21:36387213 | TTCTTTCTGAAAATA[A/G]GCATAGTTTTGTTTT | 8208 |
rs140261405 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | CHAF1B | GRCh38.p7 | 21:36403861 | AGGGTTGGGCCAAAC[A/G]GGAGGGCACTGTCTT | 8208 |
rs140294912 | snp | C/T | 0.0509478 | 0.151255 | intron-variant | CHAF1B | GRCh38.p7 | 21:36400394 | GAGAATTGCTTGAAC[C/T]TGGGAGGTGGAGGTT | 8208 |
rs140487933 | snp | C/T | 0.0588605 | 0.161139 | intron-variant | CHAF1B | GRCh38.p7 | 21:36389474 | AGCTGGGCATGGTGG[C/T]GCGCTCCTATAATCC | 8208 |
rs140557587 | snp | C/G | 0.00199481 | 0.0315187 | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36379074 | TGGCCACACACCACC[C/G]AAAAACTACCCAGAC | 8208 |
rs140609932 | snp | A/G | 1.69908e-05 | 0.00291463 | missense | CHAF1B | GRCh38.p7 | 21:36412891 | GGACGAAGGTCCAGC[A/G]ATGGTGCCTTCCTGG | 8208 |
rs140630794 | snp | A/C/G | 5.03659e-05 | 0.00501805 | CHAF1B | 21 | allele_origin=G(germline)/A(germline) | 21:36397429 | GGACAAAAGATATCA[A/C/G]TTTTTAATGAACATA | 8208 |
rs140663225 | snp | C/T | 3.29489e-05 | 0.00405874 | CHAF1B | 21 | allele_origin=T(somatic)/C(germline) | 21:36409420 | GCCACTCTTGCTGTT[C/T]GCTGCTGTCCGGTCT | 8208 |
rs140708378 | snp | A/G | 0.0494327 | 0.149241 | intron-variant | CHAF1B | GRCh38.p7 | 21:36382833 | GGCCTCAGCCTCCTG[A/G]GTAGCTGGGATTACA | 8208 |
rs140785998 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36408445 | CACGGTGCTTCAATC[A/G]AGGAATTGCCTGGAG | 8208 |
rs140797599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36394355 | GCTGGGATTACAGGC[A/G]TGAGCCACAGCACCT | 8208 |
rs140838659 | snp | A/G | 0.0588605 | 0.161139 | intron-variant | CHAF1B | GRCh38.p7 | 21:36398609 | AGGTGACCTGCCTGC[A/G]TTGGCCTCCCAAAGT | 8208 |
rs141027936 | snp | A/G | 0.000970806 | 0.0220105 | synonymous-codon | CHAF1B | GRCh38.p7 | 21:36413280 | CCGGAGGGTCACTCT[A/G]AACACACTGCAAGCC | 8208 |
rs141089741 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36410088 | CCCTCCTATCCTCCA[A/G]AGTAGCTGGGATTAC | 8208 |
rs141093317 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | CHAF1B | GRCh38.p7 | 21:36400158 | GCACTCTAGCCTGGG[C/T]GACAGAGCGAGACTC | 8208 |
rs141107977 | snp | A/G | 0.0263992 | 0.111815 | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36378820 | TAAATAAATATTGCC[A/G]TCCAAAAAAAGGTTG | 8208 |
rs141204260 | snp | C/T | 1.64996e-05 | 0.0028722 | intron-variant | CHAF1B | GRCh38.p7 | 21:36387581 | TGTTTTTCAAATGAA[C/T]GTGTTGGTATTGACA | 8208 |
rs141244906 | snp | G/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36397634 | GATTCTTTTGTTCTT[G/T]TTTTCATACTCATTC | 8208 |
rs141266003 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | CHAF1B | GRCh38.p7 | 21:36389037 | GCCTCTGAAACGCTC[C/T]AGCAGTGCCGGTCGG | 8208 |
rs141542144 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHAF1B | GRCh38.p7 | 21:36400989 | AATAGTAATGCTTCC[C/T]GGGTGCGGTGGCTCA | 8208 |
rs141607866 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36397346 | ATTTAAGTCATAGTT[C/T]ATACTATTTGGGCTC | 8208 |
rs141667193 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | CHAF1B | GRCh38.p7 | 21:36390073 | GTGCGGTGGCTCACG[C/T]CTGTAATCCCAGCAC | 8208 |
rs141779725 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHAF1B | GRCh38.p7 | 21:36410841 | ACTTTTTTTATTTTT[A/G]GTAGAGGCAGGGTTT | 8208 |
rs141782477 | in-del | -/ATTG | 0.0509478 | 0.151255 | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36378298 | GGATTATACCATATA[-/ATTG]ATAACTAAACATTTC | 8208 |
rs141789458 | snp | C/T | 0.0337553 | 0.125452 | intron-variant | CHAF1B | GRCh38.p7 | 21:36414719 | TGGGTTCAAGTGATT[C/T]TCCTACCTCAGCCTC | 8208 |
rs142014691 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36414164 | TCCATTCTTCCCCTG[A/C]AGCTGATGTCCAGTT | 8208 |
rs142060089 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHAF1B | GRCh38.p7 | 21:36411877 | GGGATTACAGGTGCG[C/T]ACCACTACGCCTGGC | 8208 |
rs142093091 | snp | A/C/G | 0.000808034 | 0.0200842 | synonymous-codon, missense, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36386218 | CATGGGACGGCTGGG[A/C/G]GGATCCACAGACTGG | 8208 |
rs142213803 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | CHAF1B | GRCh38.p7 | 21:36391832 | CAGCCTTGACTTCCC[A/G]GGCTCAAGTGATCCT | 8208 |
rs142396424 | in-del | -/TTA | 0.396461 | 0.202606 | intron-variant | CHAF1B | GRCh38.p7 | 21:36382695 | CTGTTATTATTATTA[-/TTA]TTATTATTATTTTTG | 8208 |
rs142401509 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CHAF1B | GRCh38.p7 | 21:36382212 | TCACAGTATTTCTTT[C/T]GGATTACCGAGTAGA | 8208 |
rs142402871 | in-del | -/A | 0.0242183 | 0.107343 | intron-variant | CHAF1B | GRCh38.p7 | 21:36387775 | GGGAACCAGATAGAT[-/A]ACCTGTGTGTCTTGT | 8208 |
rs142585859 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHAF1B | GRCh38.p7 | 21:36409109 | GTCCGCTTGCCTCGG[C/T]CTCCCAAAGTGCTGG | 8208 |
rs142603404 | snp | A/G | 0.0479149 | 0.147179 | downstream-variant-500B | MORC3 | GRCh38.p7 | 21:36376844 | TTCTCAGCCTGGCGC[A/G]GTGGCTCACGCCTGT | 8208 |
rs142631891 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHAF1B | GRCh38.p7 | 21:36402462 | GAGTTTTTAAAAATA[A/G]TTTTAGAACCACATA | 8208 |
rs142646501 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | CHAF1B | GRCh38.p7 | 21:36405810 | GTTATAAAGCAAGTT[A/C]TGAACAAATGGAAAG | 8208 |
rs142716888 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | CHAF1B | GRCh38.p7 | 21:36415153 | CAAGTGGGCACATCT[G/T]ACTATTTAATGCCTT | 8208 |
rs142817288 | snp | A/G | 0.000626587 | 0.017689 | synonymous-codon | CHAF1B | GRCh38.p7 | 21:36412935 | GGACGGTTACTGCTC[A/G]TTTGTGACATTTGAG | 8208 |
rs142835675 | snp | C/T | 0.00557542 | 0.0525036 | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36379852 | GTGAATATCTAGAAT[C/T]TGGCTGTAGTTCGTT | 8208 |
rs142917506 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | CHAF1B | GRCh38.p7 | 21:36416116 | GAGAGGCAAAATCGC[C/T]CCTGGTTGAGAGCCA | 8208 |
rs142921031 | in-del | -/AG | 0.0023933 | 0.0345097 | | | GRCh38.p7 | 21:36378101 | CTCACTGGGGCAAGC[-/AG]GGGGAGGGAGGGGAA | 8208 |
rs142952612 | snp | C/G/T | 0.00295833 | 0.0383469 | synonymous-codon | CHAF1B | GRCh38.p7 | 21:36413124 | CCCCGGCACGACTCC[C/G/T]CCTCAGGCCAGACAG | 8208 |
rs142993215 | snp | C/G | 0.0345262 | 0.126772 | intron-variant | CHAF1B | GRCh38.p7 | 21:36393534 | TCGGCTCACCGCAAC[C/G]TCTGCCTCCTGGGTT | 8208 |
rs143113265 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | CHAF1B | GRCh38.p7 | 21:36402085 | AACTGTCCCAGACAG[G/T]TGTTAAAGAAATGTT | 8208 |
rs143171594 | snp | G/T | 3.3583e-05 | 0.0040976 | synonymous-codon | CHAF1B | GRCh38.p7 | 21:36416318 | CCCAGAGCTAAAGCG[G/T]CCCAGACTCGATGAA | 8208 |
rs143172383 | in-del | -/CTTTCT | 0.000521422 | 0.0161381 | | | GRCh38.p7 | 21:36377516 | TCATGATGTATGTAC[-/CTTTCT]CTTTCTTTTGTTGCA | 8208 |
rs143456630 | snp | C/T | 0.0475351 | 0.146656 | intron-variant, upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36380820 | ATTCCTGGGCTCAAG[C/T]GATGCACTCCCCCAC | 8208 |
rs143543321 | snp | C/T | 0.00550679 | 0.0521831 | missense, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36386183 | ACAACAAGGAGCCCG[C/T]GTACAGCCTGGACTT | 8208 |
rs143626742 | in-del | -/G | 0.0588605 | 0.161139 | intron-variant | CHAF1B | GRCh38.p7 | 21:36395764 | TGCCAAAAGCAAGTA[-/G]TGGCTAACTCCTAAT | 8208 |
rs143663771 | snp | A/C/G | 0.0115144 | 0.0749975 | intron-variant | CHAF1B | GRCh38.p7 | 21:36409921 | TTAAAAGGAATGGAC[A/C/G]TACTCCTTTTGTTTG | 8208 |
rs143837442 | snp | C/T | 0.00122613 | 0.0247298 | missense | CHAF1B | GRCh38.p7 | 21:36413314 | AGCAAGACAACACCC[C/T]GGTAAGAACTTGTTG | 8208 |
rs143866173 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | CHAF1B | GRCh38.p7 | 21:36398198 | ATTGGGACTACGGGT[A/G]TGCACCACCACACCC | 8208 |
rs143892449 | in-del | -/A | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36388467 | TTAATTGGCTTTGGG[-/A]GTTTTTTTTTTTTTT | 8208 |
rs144050419 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CHAF1B | GRCh38.p7 | 21:36407285 | CTAGCCTGGGCAACA[A/G]AGTGAGACTCTGTCT | 8208 |
rs144063647 | snp | C/T | 0.219648 | 0.248151 | intron-variant | CHAF1B | GRCh38.p7 | 21:36401371 | TATTTTTATATTATA[C/T]ATAATATATATTTTT | 8208 |
rs144273298 | snp | C/T | 0.00438332 | 0.0466095 | utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36382025 | TCTTTTCAGACTCAA[C/T]AGGTTGGATGATGCC | 8208 |
rs144396944 | snp | A/G | 0.168135 | 0.236216 | intron-variant | CHAF1B | GRCh38.p7 | 21:36390304 | CACCATTGCACTCCA[A/G]CCTGGGCAATAAGAG | 8208 |
rs144432785 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHAF1B | GRCh38.p7 | 21:36390028 | GTGCGAATAGGATTC[C/T]GGTTAACTTAGCATG | 8208 |
rs144447243 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 21:36377835 | TGAGGAATCATTTAA[A/G]TTCTCACCTCTGGCT | 8208 |
rs144470849 | snp | C/T | 0.0505692 | 0.150756 | intron-variant | CHAF1B | GRCh38.p7 | 21:36388611 | AGCTGGGATTACAGG[C/T]GCCTGCCACCACCCC | 8208 |
rs144475501 | in-del | -/G | 0.0734156 | 0.176969 | intron-variant | CHAF1B | GRCh38.p7 | 21:36397403 | TGCGTGTGTGTGTGT[-/G]TTTTTTTGTAGGACA | 8208 |
rs144596229 | snp | C/G | 0.0263992 | 0.111815 | intron-variant | CHAF1B | GRCh38.p7 | 21:36396538 | TGTGGTAGTACATGC[C/G]TATAGTCCCAGCTAC | 8208 |
rs144617206 | snp | C/G | 0.0185938 | 0.0946107 | intron-variant | CHAF1B | GRCh38.p7 | 21:36400262 | AGGCAGGTGGATCAC[C/G]TGAGGTCAGGAGTTT | 8208 |
rs144685556 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHAF1B | GRCh38.p7 | 21:36398766 | TAATTGCATTTAATT[A/G]TATTGTTGGAACAAA | 8208 |
rs144697615 | in-del | -/A | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36396653 | ACCACACCCTGTCTC[-/A]AAAAAAAAAAGAAAA | 8208 |
rs144757817 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHAF1B | GRCh38.p7 | 21:36402293 | CTCTAGCCTGGGTGA[C/T]AGAGCGAGACTCTGT | 8208 |
rs144844278 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHAF1B | GRCh38.p7 | 21:36412715 | AGCGACTTAGCAAAT[C/T]GCGATGAAACTGCAT | 8208 |
rs144873225 | in-del | -/GATAT | 0.00199481 | 0.0315187 | utr-variant-3-prime | MORC3 | GRCh38.p7 | 21:36375378 | TAATTTTGTTTTATA[-/GATAT]GATAGGCAACAGACT | 8208 |
rs144967460 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | CHAF1B | GRCh38.p7 | 21:36413620 | TGTGGCCTTCATCTC[A/C/T]GGCCTAGTCCTGAAT | 8208 |
rs145025741 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36378212 | CTTTTGTGTGCATAC[A/G]TGCACACATTCATGT | 8208 |
rs145043768 | snp | C/T | 1.64727e-05 | 0.00286986 | missense, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36387674 | CTCGTCATACCAAAG[C/T]CGTCAATGTTGTGCG | 8208 |
rs145079377 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36410664 | GCTCCATTTTTCCTC[G/T]TGCTGCTTTCTTTTT | 8208 |
rs145088637 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | CHAF1B | GRCh38.p7 | 21:36415515 | TGCATCTTATTGGAA[C/T]CATTGTTTAAACCCG | 8208 |
rs145118140 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CHAF1B | GRCh38.p7 | 21:36397605 | TTAGCCAAGATTTAT[C/T]ATAGTCTAACTTTGA | 8208 |
rs145346949 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | CHAF1B | GRCh38.p7 | 21:36394139 | TGGAGTGTAGTGGCG[C/T]GATCTTGGCTCACTG | 8208 |
rs145356472 | snp | C/T | | | utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36382067 | CCAGGTTGGTGAGGG[C/T]GGATCTTCTGTACTC | 8208 |
rs145372971 | snp | G/T | 1.65762e-05 | 0.00287886 | synonymous-codon, intron-variant | CHAF1B | GRCh38.p7 | 21:36397476 | AGTAACCTGGGACCC[G/T]TTGGGTCAATATGTT | 8208 |
rs145410160 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | CHAF1B | GRCh38.p7 | 21:36391442 | GCACTCCAGCCTGGG[C/T]GACAGGGTGAGACTC | 8208 |
rs145472084 | snp | A/C | 0.0166325 | 0.0896639 | intron-variant | CHAF1B | GRCh38.p7 | 21:36414654 | TCTTGCTCTGTTGCC[A/C]GGGCTGGAGTGCGAT | 8208 |
rs145550179 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | CHAF1B | GRCh38.p7 | 21:36394977 | CTCAGGTGATCTGCC[C/T]GCCTCAGCCTCCCAA | 8208 |
rs145632768 | snp | C/T | 0.0577344 | 0.159793 | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36379189 | TTTCATTCTGTTGCC[C/T]AGGCTAGAGTGCAGT | 8208 |
rs145634790 | snp | A/G | 0.000149119 | 0.0086335 | synonymous-codon | CHAF1B | GRCh38.p7 | 21:36415334 | GACGGACACTCCACC[A/G]AGTTCTGTACCAACC | 8208 |
rs145654704 | snp | G/T | 1.6477e-05 | 0.00287024 | splice-donor-variant | CHAF1B | GRCh38.p7 | 21:36402852 | TGCTTCTCACGCCAG[G/T]TGTGTTTCGTAGCTT | 8208 |
rs145695485 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | CHAF1B | GRCh38.p7 | 21:36391262 | CCCTGTTGAAATGCT[C/T]GGAAGTAAATCATCC | 8208 |
rs145927687 | snp | A/G | 0.0509478 | 0.151255 | intron-variant | CHAF1B | GRCh38.p7 | 21:36392088 | CCTTCCGCAGTGTTT[A/G]TGTCCCTGGGTACTT | 8208 |
rs145983765 | snp | A/G | 0.0588605 | 0.161139 | intron-variant | CHAF1B | GRCh38.p7 | 21:36393280 | TTCTGTGGAGACAGG[A/G]TCTCACTATGTTGCC | 8208 |
rs146115510 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36393803 | CTATAGCTAATATAG[C/T]GCCAGTGGAAATTTT | 8208 |
rs146165618 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | CHAF1B | GRCh38.p7 | 21:36390400 | CTCACAACCTCATTC[A/G]TTCACTGTCCTGCTG | 8208 |
rs146237369 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CHAF1B | GRCh38.p7 | 21:36410908 | TCAGGTGATCTGCCC[A/G]CCTCAGTTTCCTCTT | 8208 |
rs146284348 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36407610 | ATTATGTGAGCATGG[A/C]GGAAATATACAGATG | 8208 |
rs146369211 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | CHAF1B | GRCh38.p7 | 21:36390147 | GAGACCAGCCTGACC[A/G]ACATGGAGAAACCTC | 8208 |
rs146528592 | snp | C/T | 0.0325976 | 0.123435 | intron-variant | CHAF1B | GRCh38.p7 | 21:36389802 | GTGTGTGTGTGTGTG[C/T]GCGCGCACGCTGATT | 8208 |
rs146538871 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | CHAF1B | GRCh38.p7 | 21:36383252 | ACAGGCACACACTAC[C/T]ACTCTGTATAGTTTT | 8208 |
rs146748600 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | CHAF1B | GRCh38.p7 | 21:36409213 | GTCATGTTGGCCAGG[A/C]TGGTCTTGAACTCCT | 8208 |
rs146875965 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | CHAF1B | GRCh38.p7 | 21:36406128 | ATAAGGCGATTTAAT[A/G]TATGACCTCAGGTGC | 8208 |
rs147134815 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant, upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36380950 | GTATTTCAGATGTAA[C/G]GTATTTCAATACATC | 8208 |
rs147239070 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36398359 | GATTTTTATTTTTAT[C/T]TTTTTTAAATTGTTT | 8208 |
rs147249259 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | CHAF1B | GRCh38.p7 | 21:36401806 | AGTGCAGTGGCACGA[C/T]CTTGGCTCACTGCAA | 8208 |
rs147344938 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CHAF1B | GRCh38.p7 | 21:36415465 | TTTGGAAATTAATGC[C/T]GCCTAATTTTAAGTC | 8208 |
rs147369174 | snp | A/G | 0.000280064 | 0.0118302 | synonymous-codon | CHAF1B | GRCh38.p7 | 21:36412986 | TTTGAAAGAGAAGCC[A/G]GTTTTGAACATGAGA | 8208 |
rs147616559 | snp | A/G | 0.0341408 | 0.126114 | intron-variant | CHAF1B | GRCh38.p7 | 21:36391459 | ACAGGGTGAGACTCC[A/G]TCTCAAAAAAAAAAA | 8208 |
rs147703501 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CHAF1B | GRCh38.p7 | 21:36394233 | AGGTGTGCACCACCA[C/T]GCCTGGCTAATTTTT | 8208 |
rs147720542 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant | CHAF1B | GRCh38.p7 | 21:36409046 | TTTTAGTAGAGATGG[C/G]GTTGCACCATGTTGG | 8208 |
rs147808620 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CHAF1B | GRCh38.p7 | 21:36411885 | AGGTGCGCACCACTA[C/T]GCCTGGCTAATTCTT | 8208 |
rs147930595 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CHAF1B | GRCh38.p7 | 21:36415898 | GCCGGGACTACAGGC[A/G]TGCGCCATCACACCC | 8208 |
rs147952403 | snp | C/T | 0.000153988 | 0.00877328 | missense, intron-variant | CHAF1B | GRCh38.p7 | 21:36397427 | TAGGACAAAAGATAT[C/T]AATTTTTAATGAACA | 8208 |
rs148007534 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHAF1B | GRCh38.p7 | 21:36400738 | GACAGCAGAGACCCA[A/G]CCAAAACACTGGTAT | 8208 |
rs148023900 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36414697 | GCTCACTGCAACCTC[C/T]GCCTTCTGGGTTCAA | 8208 |
rs148060266 | snp | A/G | 3.2956e-05 | 0.00405918 | synonymous-codon | CHAF1B | GRCh38.p7 | 21:36409458 | ACTGAGGCCAGTGGT[A/G]GAAACAGGTATCCTC | 8208 |
rs148235981 | snp | A/G | 0.000274801 | 0.0117186 | utr-variant-5-prime, upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36380185 | CATCACGCCCAGCTG[A/G]CTGTATCTTCATAAC | 8208 |
rs148268249 | in-del | -/TTAA | 0.0577344 | 0.159793 | | | GRCh38.p7 | 21:36377913 | TGCACCTCACGTTAA[-/TTAA]GTCAGCGTCCTTGGG | 8208 |
rs148277419 | snp | C/G | 3.6513e-05 | 0.00427261 | missense | CHAF1B | GRCh38.p7 | 21:36416362 | CGGAAAGTCTGGACC[C/G]TTGATGGGACCTCGG | 8208 |
rs148530128 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | CHAF1B | GRCh38.p7 | 21:36402383 | TCTCCTGGTCATCTT[C/T]CCACTGTCTGCCAGT | 8208 |
rs148571776 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CHAF1B | GRCh38.p7 | 21:36416001 | TCAAATGATCCACCC[A/G]CCTCAGCCTCCCAAA | 8208 |
rs148582638 | snp | C/T | 0.000414192 | 0.0143849 | missense | CHAF1B | GRCh38.p7 | 21:36413102 | GCAGAACCCAAGACC[C/T]CAGCAGCCCCGGCAC | 8208 |
rs148582663 | snp | C/T | 0.0588605 | 0.161139 | intron-variant | CHAF1B | GRCh38.p7 | 21:36398113 | GCTGGAGTGCAGTGG[C/T]GCAATCACAGCTCAC | 8208 |
rs148599850 | snp | A/C | 0.0379877 | 0.132479 | intron-variant | CHAF1B | GRCh38.p7 | 21:36411803 | GTGTGATCTCGTTTC[A/C]CTGCAACCTCCACCT | 8208 |
rs148757082 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CHAF1B | GRCh38.p7 | 21:36382169 | GGGTATGTCTTAGCC[C/T]GGGCAAACTGAGGCA | 8208 |
rs148803596 | snp | C/T | 0.0592355 | 0.161582 | intron-variant | CHAF1B | GRCh38.p7 | 21:36393968 | GCAGTGGCATGATCT[C/T]GGCTCACTGCAATCT | 8208 |
rs148906751 | snp | C/T | 0.0655868 | 0.168795 | intron-variant | CHAF1B | GRCh38.p7 | 21:36395143 | GAAATCTCCACCTCC[C/T]GGGTTCAAGCGATTC | 8208 |
rs148959659 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | CHAF1B | GRCh38.p7 | 21:36391415 | GTTGCAGTGAGCCAA[C/G]ATTGCGCCACTGCAC | 8208 |
rs148999632 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CHAF1B | GRCh38.p7 | 21:36409884 | TTCTTTCTTCAGGAT[A/G]TATTTTCTTGCTTAA | 8208 |
rs149034419 | in-del | -/A | | | downstream-variant-500B | MORC3 | GRCh38.p7 | 21:36377123 | GCGAAACTCCGTCTC[-/A]AAAAAAAAAGGACTT | 8208 |
rs149139435 | snp | A/C/G | 3.35027e-05 | 0.00409273 | synonymous-codon | CHAF1B | GRCh38.p7 | 21:36416303 | CGCTCAGGGCAGTCC[A/C/G]CCAGAGCTAAAGCGG | 8208 |
rs149148488 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36413542 | GGCTCCTATGCACAC[A/G]CACAGACTGTGATTT | 8208 |
rs149193400 | snp | A/C | 1.64749e-05 | 0.00287005 | missense | CHAF1B | GRCh38.p7 | 21:36399537 | GTGCTGCGAGTATAC[A/C]GTATACAGAAGAAGC | 8208 |
rs149255074 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | CHAF1B | GRCh38.p7 | 21:36390013 | CTCCCAGACTAATGT[A/G]TGCGAATAGGATTCC | 8208 |
rs149308834 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36384740 | TCCAGTAAAAGCAGC[C/G]CATCCAGAGGTACTT | 8208 |
rs149432437 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | CHAF1B | GRCh38.p7 | 21:36397836 | GGTTTCAAGCGATTC[C/T]CCTGTCTCAGCTTCC | 8208 |
rs149528015 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36411771 | TATCACTCTGTCACC[C/T]GGGCTGGAGTGCAGT | 8208 |
rs149682331 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CHAF1B | GRCh38.p7 | 21:36408526 | TCAGAACCAGGTCCC[C/T]GGGGATTGCCCACAG | 8208 |
rs149737798 | snp | A/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 21:36377482 | GAACAACTGTTGTTT[A/T]ACAGAACAACGTGGG | 8208 |
rs149779768 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36390524 | GGTGACCTCAGGCTA[A/G]AGTACCTGATATCTA | 8208 |
rs149833910 | snp | C/T | 0.123105 | 0.215401 | intron-variant | CHAF1B | GRCh38.p7 | 21:36387975 | AGGCGCCTGCCACCA[C/T]GCCCGGCTAGTTTTT | 8208 |
rs149876634 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36404017 | CCAAGAAGTCTCAGG[A/G]CTAAGAATAAGTAGT | 8208 |
rs150000465 | in-del | -/TT | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36404758 | TTTTTTTTTTTTTTT[-/TT]AAAAAGCAGAGTCTC | 8208 |
rs150199751 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36410147 | TTTGTATTTTTAGTA[A/G]AGATGGGATTTTGCC | 8208 |
rs150207094 | snp | C/T | 0.0494327 | 0.149241 | upstream-variant-2KB, intron-variant | CHAF1B | GRCh38.p7 | 21:36383893 | GACCTCATGATCCGC[C/T]CACCTCGGCCTCCTA | 8208 |
rs150259885 | snp | A/T | 0.00199481 | 0.0315187 | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36378984 | TTTTCTGTGTTTTAT[A/T]CATGTTCTTTGCCTA | 8208 |
rs150451153 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36400996 | ATGCTTCCCGGGTGC[A/G]GTGGCTCAGCCTGTA | 8208 |
rs150455108 | snp | A/G | 0.000153988 | 0.00877328 | missense, intron-variant | CHAF1B | GRCh38.p7 | 21:36397435 | AAGATATCAATTTTT[A/G]ATGAACATAAAAGTT | 8208 |
rs150591609 | snp | A/G/T | 9.88344e-05 | 0.00702912 | missense | CHAF1B | GRCh38.p7 | 21:36411522 | GCCTCGGAGGATTCC[A/G/T]TGCTTCTGTATGACA | 8208 |
rs150601499 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CHAF1B | GRCh38.p7 | 21:36415057 | GTTTTGAAACTTTTC[A/G]ATGACTGGTTATGGT | 8208 |
rs150742914 | in-del | -/A | 0.144296 | 0.226554 | intron-variant | CHAF1B | GRCh38.p7 | 21:36405957 | AGCCAAAGAAGTATT[-/A]AAAAAAAAAACAGTG | 8208 |
rs150756912 | snp | C/T | 0.000148249 | 0.00860829 | synonymous-codon, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36387636 | AGATGGAAAAGCCAT[C/T]GTGGAATTTTTGTCC | 8208 |
rs150810825 | snp | A/G | 0.00716266 | 0.059414 | intron-variant, upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36380630 | TTGTCACCCAGGCTC[A/G]AGTAGCAGTGGCGCG | 8208 |
rs150924553 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36408405 | GGGTCCTAGGGAGAA[A/C]GGAGCCTGGGCAGCT | 8208 |
rs151125026 | snp | C/G | 0.0501905 | 0.150254 | downstream-variant-500B | CHAF1B | GRCh38.p7 | 21:36417186 | GAGCGATCCTTCCAC[C/G]TCAGCTTCCCGAGTA | 8208 |
rs151197916 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | CHAF1B | GRCh38.p7 | 21:36399185 | GATTACAGGCGCCCA[C/T]CACCACGCCCGGCTA | 8208 |
rs151283516 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CHAF1B | GRCh38.p7 | 21:36389371 | AGCACTTTGGGAGAC[C/T]GAGGCAGGTGGATCA | 8208 |
rs180700914 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CHAF1B | GRCh38.p7 | 21:36383445 | TGGAAATTAAAATGC[C/T]TTGAGAAGTTTTTTT | 8208 |
rs180715182 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36385738 | TCCGGGAGGCTCCTC[C/T]CGGGGCGGGCCCCTC | 8208 |
rs180751679 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHAF1B | GRCh38.p7 | 21:36407186 | GCACACCTGTAATCC[C/T]AGCTACTCAAGAGCC | 8208 |
rs180753969 | snp | G/T | 0.00159617 | 0.0282053 | utr-variant-3-prime | MORC3 | GRCh38.p7 | 21:36375779 | TCCTGATACAACTCT[G/T]GTTATAAGTGAATTG | 8208 |
rs180771600 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | CHAF1B | GRCh38.p7 | 21:36396598 | AGTTGAGGCTGCAGT[G/T]AGCTCTGACGGCGCC | 8208 |
rs180998928 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36379412 | GCCTCCCAAATTGTT[C/G]GGATTACAGGCATTT | 8208 |
rs181002034 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36401349 | TATATTTATATTATA[C/T]ATAATATATTTTTAT | 8208 |
rs181155232 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CHAF1B | GRCh38.p7 | 21:36390468 | AGGTTACGTGGTAAT[C/T]GTAGAGTCAGAATGT | 8208 |
rs181159170 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36412291 | CTGGGCCTGTGTAGA[G/T]GATGTCACTCAGCAC | 8208 |
rs181245661 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36379629 | TTTTTAGAATTGTCT[A/G]TTGATCACAGAGTTA | 8208 |
rs181397016 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | CHAF1B | GRCh38.p7 | 21:36401984 | GGACTCAAGTGATCC[A/G]CCCGCCTTGGCCTCC | 8208 |
rs181440272 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36391027 | TGAAGGTTTCTGAGC[A/T]AGGAACATTTGCCAA | 8208 |
rs181441850 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | CHAF1B | GRCh38.p7 | 21:36412445 | GCTCACTACAACCTC[C/T]GCCTCCTGGGTTCAA | 8208 |
rs181482341 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CHAF1B | GRCh38.p7 | 21:36400833 | AGGAATCAAGGCTAC[C/T]GAGGCAGGCAGCGAG | 8208 |
rs181611223 | snp | A/G | 0.00358779 | 0.0422022 | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36378255 | TTTACATTAAATTGC[A/G]TATATTTGTGTCGAT | 8208 |
rs181653099 | snp | C/G | 0.000816593 | 0.0201898 | utr-variant-3-prime | CHAF1B | GRCh38.p7 | 21:36416391 | GGCTTCTGCTCGAAG[C/G]CTACCAGGCTCCCGG | 8208 |
rs181656166 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36384282 | TTATGTTTGAGAGAC[A/G]CGAAGAATCCAGAGC | 8208 |
rs181858456 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36394330 | TCTGCCTGCCTCGGC[C/T]TCCCAAAGTGCTGGG | 8208 |
rs181917474 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36382675 | GCTGGGATTACAGGC[A/G]CCACCACCATGCCTG | 8208 |
rs182059789 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | MORC3 | GRCh38.p7 | 21:36375631 | TTGCCCCTAAGCTTT[A/G]TGCAATTTTTTCTGG | 8208 |
rs182071159 | snp | A/C/G | 0.00199481 | 0.0315187 | downstream-variant-500B | CHAF1B | GRCh38.p7 | 21:36417171 | CGACCTCCTGGGCTC[A/C/G]AGCGATCCTTCCACC | 8208 |
rs182114550 | snp | C/T | 0.00100991 | 0.0224485 | synonymous-codon | MORC3 | GRCh38.p7 | 21:36375230 | GCAAGTGAATTACGA[C/T]GTTGATGTAGTTGAT | 8208 |
rs182344612 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36380592 | TTTAAATATATATAT[A/T]TTTTTTGAGACAGGC | 8208 |
rs182349742 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36403260 | GTCAAGAGTTCATGA[A/C]CAGCCTGGCCAACAT | 8208 |
rs182361449 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36395552 | TGACAGGCCCGGGCC[C/T]TGCCTTTATGGAGGT | 8208 |
rs182436629 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CHAF1B | GRCh38.p7 | 21:36410007 | CTTGCTCTGTCGCCC[A/G]GGCTGGAGTGCAGTG | 8208 |
rs182667174 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | CHAF1B | GRCh38.p7 | 21:36387231 | ATAGTTTTGTTTTTT[G/T]TTTTTTTTTGAGACA | 8208 |
rs182680817 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36413769 | TGTACCCTCTCTGTT[G/T]GCAGTCTTTGTGGCC | 8208 |
rs182712948 | snp | A/G | 0.0363816 | 0.129874 | intron-variant | CHAF1B | GRCh38.p7 | 21:36392512 | CGGCCGGGCAGAGGC[A/G]CCCCCCACCTCCCGG | 8208 |
rs182792520 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36380021 | CCCCACGAGTAGTAG[C/G]AACTACAGGCACATG | 8208 |
rs182972886 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36412812 | CTTGTGATTTTGCTC[A/G]AACTTCCCTCTTCTA | 8208 |
rs183200106 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36388081 | ACCTGCCTCGGCCTC[C/T]CAAAGTGTTGGGATT | 8208 |
rs183202240 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | CHAF1B | GRCh38.p7 | 21:36410747 | CTCGTTGCAGCCTTC[A/G]TCTCCCAGGTTCAAG | 8208 |
rs183268125 | snp | A/C | | | upstream-variant-2KB, intron-variant | CHAF1B | GRCh38.p7 | 21:36385222 | GGTCTGGCAGGCATA[A/C]ATTCCGGCCGGGATT | 8208 |
rs183277709 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | CHAF1B | GRCh38.p7 | 21:36408948 | CAACCTCTGCCTCCC[A/G]GGTTCAAGTGATTCT | 8208 |
rs183352960 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36414698 | CTCACTGCAACCTCC[A/G]CCTTCTGGGTTCAAG | 8208 |
rs183512099 | snp | A/C | 0.00716266 | 0.059414 | | | GRCh38.p7 | 21:36377267 | TTCCCTTCCTTTTGG[A/C]CAGCTTCTCTATGTA | 8208 |
rs183545620 | snp | A/G | 0.142947 | 0.22592 | intron-variant | CHAF1B | GRCh38.p7 | 21:36392652 | CCTCTCTTCCCAGAC[A/G]GGGCGGCTGCCGGGC | 8208 |
rs183561352 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36396870 | AACCTGTTTCACCTT[C/T]AAAATGCAGACAGCT | 8208 |
rs183786695 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | MORC3 | GRCh38.p7 | 21:36376313 | AAGTATAAACTATGT[A/G]TATATAAGAACCATA | 8208 |
rs184053803 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CHAF1B | GRCh38.p7 | 21:36397248 | CATGAAGTCATCTTT[C/G]TGACCCCAGAGCCTG | 8208 |
rs184059625 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CHAF1B | GRCh38.p7 | 21:36393522 | AATGGCATGATCTCG[C/G]CTCACCGCAACCTCT | 8208 |
rs184072637 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36416075 | TGACATTCAAAAATG[C/T]CACTAGACATTGCCC | 8208 |
rs184225329 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CHAF1B | GRCh38.p7 | 21:36412069 | CATTAAAAGGAAAGC[C/T]GTTTCTAGTTTGCCA | 8208 |
rs184417337 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36390163 | ACATGGAGAAACCTC[A/G]TCTCTACTAAAAATA | 8208 |
rs184466263 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | CHAF1B | GRCh38.p7 | 21:36382221 | TTCTTTTGGATTACC[C/G]AGTAGAATACCGTGG | 8208 |
rs184485050 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36405418 | TGCAAAATACATAGA[A/G]TAAATTTATTTATTT | 8208 |
rs184505046 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | CHAF1B | GRCh38.p7 | 21:36392810 | CTTCCTAGACGGGGT[A/G]GCGGCCGGGCAGAGG | 8208 |
rs184639156 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | CHAF1B | GRCh38.p7 | 21:36414972 | TTCTATATATAGAAA[C/T]CATATCTGACTGCCT | 8208 |
rs184645611 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | CHAF1B | GRCh38.p7 | 21:36382724 | ATTATTATTATTTTT[C/G]AGATGGAGTTCTGCT | 8208 |
rs184746570 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CHAF1B | GRCh38.p7 | 21:36406235 | CACTGAAGGCAGATA[A/G]GACAAGAGTATGTCA | 8208 |
rs184782022 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36381049 | ATGCTATTTGAAGAT[A/G]ATAATCTAGGCACAG | 8208 |
rs184897957 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CHAF1B | GRCh38.p7 | 21:36404160 | TGGAGTGCAGTGGCA[C/T]GATCTTGGCTCACCA | 8208 |
rs184991974 | snp | A/G/T | 4.96613e-05 | 0.00498283 | intron-variant | CHAF1B | GRCh38.p7 | 21:36411645 | TGAGTGAAGGAGACC[A/G/T]TGGCTGTATCCTGGA | 8208 |
rs184996037 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36378916 | TTTGCTAATTTGATA[C/T]GTGAAAATATGACAG | 8208 |
rs185000164 | snp | G/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36401072 | AGGAGTTCGAGACTA[G/T]CCTGGCTAACATGGT | 8208 |
rs185086299 | snp | A/C | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36392720 | AGAGACGCTCCTCAC[A/C]TCCCAGACAGGGCGG | 8208 |
rs185095355 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | CHAF1B | GRCh38.p7 | 21:36416621 | TTTCTGAAACTGGAG[C/T]GGTTCAACGTTATCC | 8208 |
rs185191457 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | CHAF1B | GRCh38.p7 | 21:36394913 | ATTTTTGTATTTTTA[G/T]TAGAGACGGGTTTCA | 8208 |
rs185232863 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36379535 | TATCTGCATATTTGT[C/T]TGTTGAATGTTGGTC | 8208 |
rs185237031 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36401569 | TATATTATACATAAT[A/G]TATATTTTTATATTA | 8208 |
rs185295351 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36390914 | TTCCATCTCAGCCTC[C/T]CAAAGTGCTGGCATT | 8208 |
rs185302699 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CHAF1B | GRCh38.p7 | 21:36412366 | TGCTTGGCCCAGTGT[A/G]AGGTTTTTTTTTTGA | 8208 |
rs185336082 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36399303 | TGCCTCCCAAAGTGT[C/T]GGGATTACAGGCGTG | 8208 |
rs185440357 | snp | A/G | 0.00478085 | 0.0486577 | | | GRCh38.p7 | 21:36377889 | TTTTTTAAACTCCCA[A/G]AGTCAGGCTGCACCT | 8208 |
rs185579170 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36389509 | TACTCAGGAGGCTGA[C/G]GTGGAGAATCGCTGT | 8208 |
rs185756612 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | MORC3 | GRCh38.p7 | 21:36375867 | AAGGTAAGCAAAAAC[C/G]AACTCCATTTTGCCA | 8208 |
rs185771904 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHAF1B | GRCh38.p7 | 21:36396684 | AAAAAAAGGAATGGC[C/T]AAGGCTTCATAACTC | 8208 |
rs185849085 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36384428 | TGTACTTTTAGAACA[A/G]CCATATTATCTAAAG | 8208 |
rs185849553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36408885 | TTTAGACGGAGTTTC[A/G]CTCTTGTTGCCCAGG | 8208 |
rs185949588 | snp | C/G | 0.000101151 | 0.00711094 | missense | CHAF1B | GRCh38.p7 | 21:36413240 | CCCTGCAGCCCAGTA[C/G]TCAAAACACAAAAGC | 8208 |
rs186078602 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | CHAF1B | GRCh38.p7 | 21:36392078 | GACCCAGTGGCCTTC[C/T]GCAGTGTTTGTGTCC | 8208 |
rs186158313 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHAF1B | GRCh38.p7 | 21:36402157 | TTTCTTTTTTTAAAG[A/G]GTGCATTTGTTAATA | 8208 |
rs186296638 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | MORC3 | GRCh38.p7 | 21:36375636 | CCTAAGCTTTGTGCA[A/G]TTTTTTCTGGTTCCC | 8208 |
rs186304994 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36395646 | GGTAGGTGGGATCAG[G/T]TTTCCATTTTAGAAG | 8208 |
rs186353254 | snp | C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36379691 | CTGGTTAAGAGTTAA[C/G]AAGAAACCTTTTAAA | 8208 |
rs186468072 | snp | C/T | 0.00835141 | 0.0640778 | upstream-variant-2KB, intron-variant | CHAF1B | GRCh38.p7 | 21:36383503 | TTATATCAATTTTCA[C/T]TATTAAAAAGTTCTC | 8208 |
rs186611662 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36408578 | GTAGAACTGGAGTAA[A/G]GGCTGAGAACAGACA | 8208 |
rs186626087 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36403411 | GCAGTGAGCCGAGAT[C/T]ACACCACTGTACTCC | 8208 |
rs186653355 | snp | A/G | | | utr-variant-3-prime | MORC3 | GRCh38.p7 | 21:36375486 | TTTGAAATACCTGTG[A/G]ATTGTTGGCATTGAG | 8208 |
rs186996924 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CHAF1B | GRCh38.p7 | 21:36409033 | TTAATTTTTGTATTT[C/T]TAGTAGAGATGGGGT | 8208 |
rs187058215 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CHAF1B | GRCh38.p7 | 21:36413978 | TCCAGCAGCCTGGTC[A/G]GTGAGAAACGGAGGT | 8208 |
rs187107789 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36398737 | AAGAAGTCTTGTTGT[C/T]GTGTTTACTGGCATA | 8208 |
rs187177775 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36386590 | GTGACAGAGCCAGAC[C/T]CTTCTCTTAAGTAAA | 8208 |
rs187226984 | snp | A/G | 0.0162398 | 0.0886349 | downstream-variant-500B | CHAF1B | GRCh38.p7 | 21:36417320 | CACAAGTATGTGTGT[A/G]TATATATATTTTTTT | 8208 |
rs187251447 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36391150 | CAGTGGCATTTGCTG[C/G]CCTAGGGACCCTTCT | 8208 |
rs187492125 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CHAF1B | GRCh38.p7 | 21:36388515 | ACTGTTATCTAGGCT[A/G]GAGTGCAGTGGCACA | 8208 |
rs187495511 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | CHAF1B | GRCh38.p7 | 21:36411199 | GCTCACTGCAACCTC[C/T]GCCTCCTGGGTTCAA | 8208 |
rs187550395 | snp | A/T | 0.000798403 | 0.0199641 | downstream-variant-500B | MORC3 | GRCh38.p7 | 21:36377119 | AAACTCCGTCTCAAA[A/T]AAAAAGGACTTTTCT | 8208 |
rs187559950 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36380903 | TTTGTTTTTTTTGTT[C/T]GTTTGTTTTTCTGTA | 8208 |
rs187622033 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36414980 | ATAGAAACCATATCT[G/T]ACTGCCTTTTACAGC | 8208 |
rs187623998 | snp | G/T | 0.0456553 | 0.144025 | intron-variant | CHAF1B | GRCh38.p7 | 21:36397402 | GGTGCGTGTGTGTGT[G/T]TTTTTTTTGTAGGAC | 8208 |
rs187824366 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36380208 | TTCATAACAAAATGT[A/G]ATGGTGTTTTATATT | 8208 |
rs187874226 | snp | C/G | 0.0162398 | 0.0886349 | intron-variant | CHAF1B | GRCh38.p7 | 21:36404290 | ATTTTTAGTAGAGAC[C/G]GGGTTTCACCATGTT | 8208 |
rs187888857 | snp | C/T | 0.00042876 | 0.0146354 | intron-variant | CHAF1B | GRCh38.p7 | 21:36402902 | GCCGAGTGGGGATGT[C/T]TGCTCCCGTTTTACG | 8208 |
rs188110644 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CHAF1B | GRCh38.p7 | 21:36387976 | GGCGCCTGCCACCAC[A/G]CCCGGCTAGTTTTTT | 8208 |
rs188148359 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36381188 | TACAATGGCATAATC[A/G]TAGCTCACTACATCC | 8208 |
rs188185037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36393072 | CGAAAACCAGACAGG[C/T]GTGGCGGCGTGCGCC | 8208 |
rs188370422 | snp | A/C | 0.00191074 | 0.0308499 | | | GRCh38.p7 | 21:36377382 | TGATTCTTTGGAAGC[A/C]CTTAGATACTTTTTG | 8208 |
rs188410790 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | CHAF1B | GRCh38.p7 | 21:36410182 | TGGCCAGGCTGGTCT[C/T]GAACTCCTGACCTCA | 8208 |
rs188411329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36393913 | TTTTTGTTTTGTTTT[A/G]TTTAGAGTCAGAGTC | 8208 |
rs188413283 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36416113 | CTTGAGAGGCAAAAT[C/T]GCCCCTGGTTGAGAG | 8208 |
rs188615001 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CHAF1B | GRCh38.p7 | 21:36397206 | ATGGGTCTGTCTGAT[C/T]TGTGGGCTCCCTGAG | 8208 |
rs188724483 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | CHAF1B | GRCh38.p7 | 21:36390348 | CAAAAAAAAAAAAAA[A/G]AAAGAAAGAAAAACA | 8208 |
rs188921659 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36392656 | TCTTCCCAGACGGGG[C/T]GGCTGCCGGGCGGAG | 8208 |
rs188938581 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36390945 | ACAGGCGTGAGCCAC[C/T]CCACCCTGCCTATTA | 8208 |
rs188955722 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36412437 | CGATCGTGGCTCACT[A/G]CAACCTCCGCCTCCT | 8208 |
rs189165739 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CHAF1B | GRCh38.p7 | 21:36414765 | TACAGGCATGCGCCA[C/T]CATGCCTGGCTGACT | 8208 |
rs189208632 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36383189 | CAAGTCCCGGGTTCA[A/G]TGGATTCTCTTGCCT | 8208 |
rs189327010 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36379405 | CTTCTGGGCCTCCCA[A/G]ATTGTTGGGATTACA | 8208 |
rs189342403 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CHAF1B | GRCh38.p7 | 21:36401209 | GAGGTGGAGTTTGCG[A/G]TGAGCCGAGATTGCG | 8208 |
rs189462132 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36406669 | ATATGTTGTGGAATG[A/G]CTAAATCTAGCTAAT | 8208 |
rs189505989 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CHAF1B | GRCh38.p7 | 21:36408598 | GAGAACAGACAGTGC[C/T]GGAATATATGTTTTT | 8208 |
rs189581175 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | CHAF1B | GRCh38.p7 | 21:36382425 | TTAGACAGTGCTGAA[C/G]AGTTTTCTAAAGTAT | 8208 |
rs189583302 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36405869 | TAATTTCATTTCCAA[A/T]TAGAATTGCATTAAA | 8208 |
rs189717073 | snp | C/T | 0.00279162 | 0.0372561 | upstream-variant-2KB, intron-variant | CHAF1B | GRCh38.p7 | 21:36383762 | CACGCCATTGTCTTG[C/T]CTCAGCCTCCCGAGT | 8208 |
rs189850219 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | MORC3 | GRCh38.p7 | 21:36375754 | GGATTTTTAAATAAT[G/T]TAGTAACACTCCTGA | 8208 |
rs189858867 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CHAF1B | GRCh38.p7 | 21:36396145 | GCTGGGATTACAGGC[A/G]CCCGCCACCACTCCC | 8208 |
rs189927002 | snp | C/T | 0.0115144 | 0.0749975 | downstream-variant-500B | CHAF1B | GRCh38.p7 | 21:36417321 | ACAAGTATGTGTGTA[C/T]ATATATATTTTTTTT | 8208 |
rs190011605 | snp | A/G | 0.00517822 | 0.0506191 | | | GRCh38.p7 | 21:36378081 | GGGATCAGCATATCC[A/G]CTTTCTCACTGGGGC | 8208 |
rs190031675 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CHAF1B | GRCh38.p7 | 21:36412070 | ATTAAAAGGAAAGCC[A/G]TTTCTAGTTTGCCAC | 8208 |
rs190190964 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36396746 | GCTAAATATTTTCCC[C/T]GAAGTCCCTTTTCCA | 8208 |
rs190238112 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | CHAF1B | GRCh38.p7 | 21:36411966 | ACTCCTGGGCTCAAC[G/T]ATCCTCCTGCCCCAG | 8208 |
rs190280606 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36400101 | AGAATCACCTGAACC[A/T]GGGAGGCGGAGGTCT | 8208 |
rs190410609 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | CHAF1B | GRCh38.p7 | 21:36392265 | ATAGATTAGCAGCAT[C/T]CCAAGGCAGAAGAAT | 8208 |
rs190415268 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36413407 | GGTGAAATTTCAGGC[A/G]GTGAATGCTTCATGC | 8208 |
rs190579457 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHAF1B | GRCh38.p7 | 21:36394920 | TATTTTTAGTAGAGA[C/T]GGGTTTCATCATGTT | 8208 |
rs190687379 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | CHAF1B | GRCh38.p7 | 21:36414175 | CCTGCAGCTGATGTC[C/T]AGTTACCCCTCTGAT | 8208 |
rs190799419 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36380496 | CCCCAGGCTGGTCTC[A/C]AGAACTTCTGGGCTC | 8208 |
rs190804908 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | CHAF1B | GRCh38.p7 | 21:36402945 | AGCTCAGTGAATGCT[G/T]ATTAGAGTGGGGGTC | 8208 |
rs190820022 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | MORC3 | GRCh38.p7 | 21:36375560 | GTAATTAAGCCTGCA[C/T]ATATTTTTTTATTGC | 8208 |
rs190836496 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | CHAF1B | GRCh38.p7 | 21:36417170 | TCGACCTCCTGGGCT[C/T]GAGCGATCCTTCCAC | 8208 |
rs190864974 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CHAF1B | GRCh38.p7 | 21:36387060 | TTATTGTAACTGGAC[A/G]TTCATTGTTTTGGGA | 8208 |
rs191039884 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | CHAF1B | GRCh38.p7 | 21:36385173 | ATGGATAATAATAAT[A/G]AATAATAATGAATCC | 8208 |
rs191044264 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36408914 | GGCTGGAGTGCAATG[A/G]TGCGATCTCTGCTCA | 8208 |
rs191088716 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | CHAF1B | GRCh38.p7 | 21:36393214 | GTGGAGAGAGCGGGA[C/G]AGGGAGAGGGAGACG | 8208 |
rs191102687 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | CHAF1B | GRCh38.p7 | 21:36415575 | GCACCTGGCCAGTGA[G/T]AGCATCCTGGTGAGC | 8208 |
rs191115896 | snp | G/T | 0.0150606 | 0.0854603 | intron-variant | CHAF1B | GRCh38.p7 | 21:36409859 | AATACATGTCAGTTT[G/T]TTTTTTTTTTTCTTT | 8208 |
rs191124898 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | MORC3 | GRCh38.p7 | 21:36375952 | GAATGAAGAAACAGT[C/T]TTTAACAGAAAAAAG | 8208 |
rs191341082 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | CHAF1B | GRCh38.p7 | 21:36398472 | TCAAGCGATTCTCCT[A/G]CCTCATCCTCCTGAG | 8208 |
rs191372185 | snp | C/T | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 21:36377192 | AGCAGCTATGTAAAT[C/T]ATATGTAAGTTTTGT | 8208 |
rs191410027 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CHAF1B | GRCh38.p7 | 21:36397233 | TGAGGGTGGGGACTG[C/T]ATGAAGTCATCTTTG | 8208 |
rs191603469 | snp | A/G | 0.0023933 | 0.0345097 | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36379940 | TGCCCAGGCTGGAGT[A/G]CAGTGGCATGATCAC | 8208 |
rs191614469 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36379590 | AATATCTGATTGGCG[A/T]AGAGGAAAAAATAAA | 8208 |
rs191707857 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36388058 | GAACTCCTGACCTCA[A/G]GTGATCCACCTGCCT | 8208 |
rs191921891 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | CHAF1B | GRCh38.p7 | 21:36412504 | AGCTGGGATTACAGG[C/T]GCCCACCACCATGGC | 8208 |
rs191954596 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | CHAF1B | GRCh38.p7 | 21:36402226 | TGAGACGGGAGGATT[G/T]CTTTGAGCCCAGAAG | 8208 |
rs191957322 | snp | C/G | 8.26235e-05 | 0.00642689 | intron-variant | CHAF1B | GRCh38.p7 | 21:36411629 | TGCTAATGAGGGAGA[C/G]TGAGTGAAGGAGACC | 8208 |
rs191994267 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CHAF1B | GRCh38.p7 | 21:36388759 | GGCGTGAGCCACCGC[A/G]CCCGGGCTATTTGGG | 8208 |
rs192176202 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36403986 | ACTGCGGAACATGTG[C/T]GAATGACACTTTGGC | 8208 |
rs192215629 | snp | G/T | 0.00478085 | 0.0486577 | utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36382044 | TTGGATGATGCCCCA[G/T]ATACTGCCCAGGTTG | 8208 |
rs192219894 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36391443 | CACTCCAGCCTGGGC[A/G]ACAGGGTGAGACTCC | 8208 |
rs192260742 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36392646 | GGGGCTCCTCTCTTC[C/T]CAGACGGGGCGGCTG | 8208 |
rs192391465 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CHAF1B | GRCh38.p7 | 21:36389835 | TAGAGGGAAAAGTGG[A/G]GAGCAGGAGCGCCAC | 8208 |
rs192485103 | snp | A/G | | | downstream-variant-500B | MORC3 | GRCh38.p7 | 21:36377054 | TGGGAGGTGGAGGTT[A/G]CAGCGAGCCGAGATC | 8208 |
rs192515946 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHAF1B | GRCh38.p7 | 21:36405942 | ATAAATGCTGAAGAA[C/T]AGCCAAAGAAGTATT | 8208 |
rs192543803 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36381047 | AAATGCTATTTGAAG[A/G]TAATAATCTAGGCAC | 8208 |
rs192645203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36410511 | ATTTTGGAAGTCTCT[A/G]TAGCTGTGTTTTGAG | 8208 |
rs192694888 | snp | C/T | 0.00478085 | 0.0486577 | | | GRCh38.p7 | 21:36377516 | TCATGATGTATGTAC[C/T]TTTCTCTTTCTTTTG | 8208 |
rs192778730 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36412030 | ACCACGCCCGGCCCC[A/G]ATTTTGTTTTTTAAA | 8208 |
rs192903940 | snp | A/C/T | 0.0154538 | 0.0865337 | intron-variant | CHAF1B | GRCh38.p7 | 21:36399282 | CTCAAGTGATTCACC[A/C/T]GCCTCTGCCTCCCAA | 8208 |
rs193921141 | snp | A/G | | | missense | CHAF1B | GRCh38.p7 | 21:36409408 | GCTGT[A/G] | 8208 |
rs199603853 | snp | A/G | 8.27123e-05 | 0.00643034 | intron-variant | CHAF1B | GRCh38.p7 | 21:36411418 | TGCACCTGGTCAGAA[A/G]CCTTGTTTCTGTGGT | 8208 |
rs199627494 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36382694 | CCACCATGCCTGGCT[A/G]TTATTATTATTATTA | 8208 |
rs199657347 | snp | C/T | 8.23621e-05 | 0.00641672 | synonymous-codon | CHAF1B | GRCh38.p7 | 21:36411521 | GGCCTCGGAGGATTC[C/T]GTGCTTCTGTATGAC | 8208 |
rs199719028 | snp | C/T | 1.64844e-05 | 0.00287087 | missense, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36394597 | CAACTGATGGGAATT[C/T]AATGGCTTCTGCCTC | 8208 |
rs199830097 | snp | A/G | 8.25294e-05 | 0.00642323 | intron-variant | CHAF1B | GRCh38.p7 | 21:36409342 | TTGCTTAGTCACAGT[A/G]CCTTTTCCTAACACT | 8208 |
rs199857685 | in-del | -/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36409968 | TCAATTTTCTTTTTC[-/T]TTTTTTTTTTTTTGA | 8208 |
rs199888379 | snp | C/T | 0.000263622 | 0.0114779 | intron-variant | CHAF1B | GRCh38.p7 | 21:36402860 | ACGCCAGGTGTGTTT[C/T]GTAGCTTTGGACTTA | 8208 |
rs199898351 | snp | G/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36388347 | CATCCCAAGCAAGGC[G/T]ACTGTTCTGGTTTTG | 8208 |
rs199981627 | in-del | -/TTTCTTTTTTTTTT | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36382535 | CTATTTTTCTTTTTC[-/TTTCTTTTTTTTTT]TTTTTTTTTCAGACT | 8208 |
rs200144938 | snp | C/G | 0.00218957 | 0.033015 | synonymous-codon | CHAF1B | GRCh38.p7 | 21:36411590 | ACATTACCACACCCT[C/G]AGTGACATTTCATGG | 8208 |
rs200157692 | snp | C/T | 0.00233818 | 0.0341119 | intron-variant | CHAF1B | GRCh38.p7 | 21:36399507 | GTGGTAAATCAGACA[C/T]GTTCTTTCTTCAGGG | 8208 |
rs200198213 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36415414 | ATTGTTACTGGTTTA[A/G]TATAATGAAAGGTAG | 8208 |
rs200218353 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36390338 | AACACCATCTCAAAA[A/G]AAAAAAAAAAAAAGA | 8208 |
rs200304218 | snp | A/G | 0.000189876 | 0.00974177 | missense | CHAF1B | GRCh38.p7 | 21:36416343 | GATGAAAACAAAGGA[A/G]GCACGGAAAGTCTGG | 8208 |
rs200414790 | in-del | -/G | | | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36379865 | ATTTGGCTGTAGTTC[-/G]TTTTTTTTTTTTTTT | 8208 |
rs200436991 | snp | C/G | 1.64779e-05 | 0.00287031 | synonymous-codon | CHAF1B | GRCh38.p7 | 21:36408798 | AAATGTAATGAATAC[C/G]ACTTATGTTTTCTCC | 8208 |
rs200585395 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36398417 | CTGGCTGGAATGCAG[C/T]GGTGCGATCTCGGCA | 8208 |
rs200643242 | snp | C/T | 3.30535e-05 | 0.00406518 | synonymous-codon | CHAF1B | GRCh38.p7 | 21:36412923 | CATTTCTTCCACGGA[C/T]GGTTACTGCTCATTT | 8208 |
rs200679657 | in-del | -/T | 0.0401147 | 0.135824 | intron-variant, upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36380335 | AATTTGAGTATAGAA[-/T]TTTTTTCTGTTCTAG | 8208 |
rs200693299 | snp | C/T | 0.00199792 | 0.0315431 | intron-variant | CHAF1B | GRCh38.p7 | 21:36411419 | GCACCTGGTCAGAAG[C/T]CTTGTTTCTGTGGTT | 8208 |
rs200840491 | snp | C/G/T | 0.00019846 | 0.00995957 | missense | CHAF1B | GRCh38.p7 | 21:36415360 | CAACCAGTGTGATTT[C/G/T]CACCCCTTCTACAGA | 8208 |
rs200843761 | snp | C/G | 0.00206283 | 0.0320494 | intron-variant | CHAF1B | GRCh38.p7 | 21:36397390 | TAATGCTGTTTTGGT[C/G]CGTGTGTGTGTGTTT | 8208 |
rs200971946 | snp | A/G | 0.00199792 | 0.0315431 | intron-variant | CHAF1B | GRCh38.p7 | 21:36413326 | CCCCGGTAAGAACTT[A/G]TTGGAACAAGATGTC | 8208 |
rs201004562 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36408717 | TGAACAGTTTGCTGA[A/G]ACAGTGACTTTTCTT | 8208 |
rs201096817 | snp | A/T | 0.000251103 | 0.0112022 | intron-variant | CHAF1B | GRCh38.p7 | 21:36402727 | GAAAACAAACAAAAA[A/T]AATAATAAAAATAAA | 8208 |
rs201145989 | snp | A/G/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36396816 | TCTCCTGGTCTACTC[A/G/T]GTCACCTCCTAACTA | 8208 |
rs201178033 | in-del | -/TT | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36411117 | TTCTTATAAATATTC[-/TT]TTTTTTTTTTTTTGT | 8208 |
rs201186457 | in-del | -/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36399037 | AATGTGACTTACCAA[-/T]TTTTTTTTTTTTTTT | 8208 |
rs201221145 | in-del | -/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36412369 | TGGCCCAGTGTGAGG[-/T]TTTTTTTTTTGAAAC | 8208 |
rs201247343 | snp | A/G | | | downstream-variant-500B | CHAF1B | GRCh38.p7 | 21:36417167 | GCCTCGACCTCCTGG[A/G]CTCGAGCGATCCTTC | 8208 |
rs201258713 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36390352 | AAAAAAAAAAAAAAA[A/G]AAAGAAAAACAAAGA | 8208 |
rs201339256 | snp | C/T | 1.64735e-05 | 0.00286993 | missense | CHAF1B | GRCh38.p7 | 21:36399552 | AGTATACAGAAGAAG[C/T]GTGTGGCTTTCAATG | 8208 |
rs201352644 | snp | A/G | 0.000319846 | 0.012642 | intron-variant | CHAF1B | GRCh38.p7 | 21:36397374 | CTCAAACAGGTTTTG[A/G]TAATGCTGTTTTGGT | 8208 |
rs201430464 | in-del | -/GAAAG | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36390352 | AAAAAAAAAAAAAAA[-/GAAAG]AAAAACAAAGAATGG | 8208 |
rs201455139 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36394524 | GAGTAATTGCTTTTT[C/T]CCTCTTTGTTTTTGG | 8208 |
rs201486922 | snp | A/G | 8.38863e-05 | 0.00647581 | synonymous-codon | CHAF1B | GRCh38.p7 | 21:36413205 | CAAAAGCCCCTTGCC[A/G]GGGCCTTCGGAGGAG | 8208 |
rs201581262 | snp | C/G | 6.60611e-05 | 0.00574684 | missense | CHAF1B | GRCh38.p7 | 21:36413080 | CCGGTAGAGGGAACC[C/G]CTGCCAGCAGAACCC | 8208 |
rs201612942 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36415423 | GGTTTAATATAATGA[A/G]AGGTAGAGTATCTTT | 8208 |
rs201731956 | snp | A/G | 1.64863e-05 | 0.00287104 | missense, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36394602 | GATGGGAATTTAATG[A/G]CTTCTGCCTCTGTGG | 8208 |
rs201771486 | in-del | -/AT | 0.154329 | 0.23097 | intron-variant | CHAF1B | GRCh38.p7 | 21:36389758 | AGAGTGCATGAAGGG[-/AT]ATGTGTGTGTGTGTG | 8208 |
rs201805865 | in-del | -/TTTTTTT | | | intron-variant, upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36381111 | TTTTTCTTCTTCTTC[-/TTTTTTT]TTTTTTTTTTTTTTT | 8208 |
rs201910463 | in-del | -/A | 0.0475351 | 0.146656 | intron-variant, upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36380802 | GCCCAGGCTGGTCTC[-/A]AAATTCCTGGGCTCA | 8208 |
rs201944985 | snp | A/G | 0.000131824 | 0.00811755 | missense | CHAF1B | GRCh38.p7 | 21:36408805 | ATGAATACCACTTAT[A/G]TTTTCTCCAGGAAGA | 8208 |
rs201948252 | snp | C/T | 6.59315e-05 | 0.0057412 | intron-variant | CHAF1B | GRCh38.p7 | 21:36391687 | ACTTGGGAGGGACCA[C/T]GGCAGTGATCTCTGT | 8208 |
rs201964602 | snp | C/T | 3.48299e-05 | 0.00417297 | missense | CHAF1B | GRCh38.p7 | 21:36416347 | AAAACAAAGGAGGCA[C/T]GGAAAGTCTGGACCC | 8208 |
rs202003065 | snp | C/T | 0.000636164 | 0.0178235 | intron-variant | MORC3 | GRCh38.p7 | 21:36375114 | AACTTGTAATGCTCA[C/T]CTAATAAGTTACATA | 8208 |
rs202027520 | in-del | -/AG | 0.0107246 | 0.0724382 | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36379480 | CAGTGTCTCATAAAC[-/AG]GGACTCACTGAAGTG | 8208 |
rs202049867 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36396370 | CCTCAAAAAAAAAAA[A/G]AAAAAAAAAAAAAGA | 8208 |
rs202093155 | snp | C/G/T | 0.000529587 | 0.0162648 | utr-variant-3-prime | CHAF1B | GRCh38.p7 | 21:36416405 | GCCTACCAGGCTCCC[C/G/T]GTGTGTGCAGGGAGA | 8208 |
rs202224920 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36382538 | TTTTTCTTTTTCTTT[C/T]TTTTTTTTTTTTTTT | 8208 |
rs202230102 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36398029 | ATGCCCCGCCCTGAA[C/T]TTAGTAAATCTTTAT | 8208 |
rs367543500 | in-del | -/C | | | intron-variant, upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36381135 | TTTTTTTTTTTTTTT[-/C]TTTTGCGACAGGTCT | 8208 |
rs367547379 | snp | G/T | | | upstream-variant-2KB, intron-variant | CHAF1B | GRCh38.p7 | 21:36385079 | CTCCAAGTGCCCAGC[G/T]CCAGCATAGGGTCTG | 8208 |
rs367566058 | snp | C/G/T | 0.000153988 | 0.00877328 | intron-variant | CHAF1B | GRCh38.p7 | 21:36387767 | AGATTCTTCGGGAAC[C/G/T]AGATAGATACCTGTG | 8208 |
rs367688753 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36406972 | TCTTGTAAGGAAATA[C/T]AGGAGGACATTCTAG | 8208 |
rs367699939 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | CHAF1B | GRCh38.p7 | 21:36388450 | TAGGACTGTGTTAGT[A/C]ATTAATTGGCTTTGG | 8208 |
rs367799372 | snp | A/C | 0.000232165 | 0.0107717 | intron-variant | CHAF1B | GRCh38.p7 | 21:36415418 | TTACTGGTTTAATAT[A/C]ATGAAAGGTAGAGTA | 8208 |
rs367810420 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36378952 | ATTTGTCTCAGTCCT[C/T]ACATTGGCCATTTTA | 8208 |
rs367837612 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36395899 | GCCACCGCAGCACTG[C/T]GTCAGCCCAGTTCTC | 8208 |
rs367999820 | snp | C/T | 0.000922691 | 0.0214591 | intron-variant | CHAF1B | GRCh38.p7 | 21:36391685 | TAACTTGGGAGGGAC[C/T]ATGGCAGTGATCTCT | 8208 |
rs368042028 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36396877 | TTCACCTTTAAAATG[C/T]AGACAGCTTCTCAGC | 8208 |
rs368124776 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36410206 | GACCTCAGGTGATCC[A/G]CCCACCTTGGCCTCC | 8208 |
rs368209090 | snp | A/G | 3.31109e-05 | 0.00406871 | utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36386097 | TTGAAGAAGTAGAAC[A/G]GTGCCCGAGAAACGT | 8208 |
rs368230835 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36416120 | GGCAAAATCGCCCCT[A/G]GTTGAGAGCCACTCT | 8208 |
rs368254916 | snp | C/G | 1.65715e-05 | 0.00287845 | intron-variant | CHAF1B | GRCh38.p7 | 21:36399656 | TTTAACTGAGACTTA[C/G]GAAGTCATGAGCTCC | 8208 |
rs368278276 | in-del | -/C | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36411116 | ATTCTTATAAATATT[-/C]TTTTTTTTTTTTTTT | 8208 |
rs368404227 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CHAF1B | GRCh38.p7 | 21:36414271 | AGAGCTGGGAAGGGG[A/G]ATGCAGAGGGGAGTG | 8208 |
rs368546412 | snp | G/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36397370 | TGGGCTCAAACAGGT[G/T]TTGGTAATGCTGTTT | 8208 |
rs368588534 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36402661 | ATAGCAGTTGGGAAG[C/T]GTTTATTTGTGAGTG | 8208 |
rs368592238 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36389069 | GTAAGATCCCGCGTC[A/G]GTACCCAGCTTGGCA | 8208 |
rs368595174 | snp | A/T | | | downstream-variant-500B | CHAF1B | GRCh38.p7 | 21:36417161 | ACTGCAGCCTCGACC[A/T]CCTGGGCTCGAGCGA | 8208 |
rs368616207 | snp | C/T | 1.65444e-05 | 0.00287609 | intron-variant | CHAF1B | GRCh38.p7 | 21:36391543 | ACTGTTACTGAATCA[C/T]CCTGCAGATGCTGTC | 8208 |
rs368621019 | snp | C/T | 5.03647e-05 | 0.00501795 | missense | CHAF1B | GRCh38.p7 | 21:36413204 | TCAAAAGCCCCTTGC[C/T]GGGGCCTTCGGAGGA | 8208 |
rs368629488 | snp | A/T | | | upstream-variant-2KB, intron-variant | CHAF1B | GRCh38.p7 | 21:36383785 | TCCCGAGTAGCTGGG[A/T]CTACAGGCGCCCGCC | 8208 |
rs368857178 | snp | G/T | 9.93361e-05 | 0.00704686 | intron-variant | CHAF1B | GRCh38.p7 | 21:36394532 | GCTTTTTTCCTCTTT[G/T]TTTTTGGATTCTAGG | 8208 |
rs368871516 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CHAF1B | GRCh38.p7 | 21:36397902 | CCGGTTAATTTTTGT[A/G]TTTTTAGTAGAGACA | 8208 |
rs368878509 | snp | A/G | | | downstream-variant-500B | MORC3 | GRCh38.p7 | 21:36377065 | GGTTGCAGCGAGCCG[A/G]GATCACACCATTGCA | 8208 |
rs368941131 | snp | G/T | 0.000153988 | 0.00877328 | intron-variant | CHAF1B | GRCh38.p7 | 21:36402873 | TTCGTAGCTTTGGAC[G/T]TAAAGGAATGATGGC | 8208 |
rs368965597 | snp | C/G | | | intron-variant, upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36380708 | CACCTCAGCCTCCTG[C/G]GTAGCCAGGACCACA | 8208 |
rs369007667 | snp | C/T | | | utr-variant-3-prime | MORC3 | GRCh38.p7 | 21:36375997 | AATGGCCACCAAGTT[C/T]ACTTTGAAGCCCATT | 8208 |
rs369040613 | snp | C/G | 1.65669e-05 | 0.00287805 | missense | CHAF1B | GRCh38.p7 | 21:36415336 | CGGACACTCCACCAA[C/G]TTCTGTACCAACCAG | 8208 |
rs369164121 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36401248 | CTCCAGCCTGGGCAA[C/T]AAGAGCGAAACTCTG | 8208 |
rs369167961 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | CHAF1B | GRCh38.p7 | 21:36386286 | GGGCAGAGATAGACA[C/T]CCGGGAACACTGCTT | 8208 |
rs369251042 | snp | C/T | | | synonymous-codon | CHAF1B | GRCh38.p7 | 21:36413088 | GGGAACCCCTGCCAG[C/T]AGAACCCAAGACCCC | 8208 |
rs369387426 | snp | C/G | 0.000330464 | 0.01285 | intron-variant | CHAF1B | GRCh38.p7 | 21:36409502 | TGTGTTATGTTTTCT[C/G]TCCGAAACAGGTCAC | 8208 |
rs369391435 | snp | C/T | 0.000495556 | 0.0157332 | synonymous-codon, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36386241 | CAGACTGGCGTCTGC[C/T]GGCGTGGACACCAAT | 8208 |
rs369456414 | snp | A/G | 1.64844e-05 | 0.00287087 | synonymous-codon, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36394598 | AACTGATGGGAATTT[A/G]ATGGCTTCTGCCTCT | 8208 |
rs369471237 | snp | A/C | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36389583 | GCACTCCAGCCTGGG[A/C]AACAGAGTGAGAGTC | 8208 |
rs369500459 | snp | C/T | | | intron-variant, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36381476 | TAAAAGAGACTATAA[C/T]ATAGTCTCTTTTGCT | 8208 |
rs369515812 | snp | C/G/T | 0.000150997 | 0.00868785 | intron-variant | CHAF1B | GRCh38.p7 | 21:36408876 | TACATTTTTTTTAGA[C/G/T]GGAGTTTCGCTCTTG | 8208 |
rs369638082 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36403717 | TCCCTATGTCCCTAG[A/G]AAGGCAAGGGGCTCA | 8208 |
rs369658034 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | MORC3 | GRCh38.p7 | 21:36375424 | TCTTTACTGTATTCT[A/G]TGCATTCAAATGTGG | 8208 |
rs369727402 | snp | C/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36409091 | AACTGCTGACCTCAA[C/G]TGGTCCGCTTGCCTC | 8208 |
rs369736957 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36401046 | CAGAGGTGGGCAGAT[C/T]ACCTGAGGTCAGGAG | 8208 |
rs369800241 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36404971 | CTGGTCCCAAACTCC[C/T]GACCTCAGGTGATCT | 8208 |
rs369953335 | snp | C/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36414941 | TTTAAAAAAGTATTA[C/G]CTGTGTTTCGACGCT | 8208 |
rs369971894 | snp | A/G | 0.00256528 | 0.035722 | intron-variant | CHAF1B | GRCh38.p7 | 21:36416239 | CTTCCAGAATTCTTC[A/G]TTTACTTGCCAACCT | 8208 |
rs370114112 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | CHAF1B | GRCh38.p7 | 21:36395370 | TTTAACTTTAAAAGC[A/G]ACACAAAAAATTGTT | 8208 |
rs370147714 | in-del | -/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36387268 | ACTCTGTCGCCCAGG[-/G]CTGGAGTGCAGTGGC | 8208 |
rs370155084 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | CHAF1B | GRCh38.p7 | 21:36394307 | GTCTCGATCTCCCGA[A/C]CTTGTGATCTGCCTG | 8208 |
rs370311907 | snp | C/G | | | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36378620 | AATCACTTAACCCCA[C/G]GAGGCAGAGGTTGCA | 8208 |
rs370336150 | snp | C/T | 1.64732e-05 | 0.0028699 | synonymous-codon | CHAF1B | GRCh38.p7 | 21:36411563 | CTTCCCTTTTGGTTA[C/T]GTGTCTAATATACAT | 8208 |
rs370336375 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36382612 | TGGCATGATCTTGGC[C/T]CACTGCCCTCTGGGT | 8208 |
rs370357354 | snp | A/C/G | 6.59375e-05 | 0.00574153 | intron-variant | CHAF1B | GRCh38.p7 | 21:36387770 | TTCTTCGGGAACCAG[A/C/G]TAGATACCTGTGTGT | 8208 |
rs370393464 | snp | A/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36391337 | CTAAAAATCCTGACA[A/T]GCAGCTAATTTTTTT | 8208 |
rs370521957 | in-del | -/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36394731 | CTAACTTGCTTTAAC[-/T]TTTTTTTTTTTTTTT | 8208 |
rs370567251 | snp | A/C | | | upstream-variant-2KB, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36384225 | GGTGGGCAGATTATT[A/C]ATTTGTGAATGAACA | 8208 |
rs370593673 | snp | G/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36399227 | TTTTGGTAGAGATGG[G/T]GTTTCACCATGTTGG | 8208 |
rs370632953 | snp | G/T | 3.29516e-05 | 0.00405891 | intron-variant | CHAF1B | GRCh38.p7 | 21:36387755 | GCTGTCCTTCAGAGA[G/T]TCTTCGGGAACCAGA | 8208 |
rs370636095 | in-del | -/T | | | upstream-variant-2KB, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36384300 | AAGAATCCAGAGCTT[-/T]CCAAAACAGACTGAT | 8208 |
rs370681660 | snp | A/G/T | 8.2367e-05 | 0.006417 | synonymous-codon, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36387717 | TGGGGAAATTTTAGC[A/G/T]TCGGGAGGAGATGGT | 8208 |
rs370746730 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | CHAF1B | GRCh38.p7 | 21:36396010 | TTTGTGTGGTTTTTT[A/T]TTTTATTTTAGATGG | 8208 |
rs370748276 | snp | C/T | 0.000115914 | 0.00761207 | intron-variant | CHAF1B | GRCh38.p7 | 21:36411644 | GTGAGTGAAGGAGAC[C/T]GTGGCTGTATCCTGG | 8208 |
rs370898560 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36391458 | GACAGGGTGAGACTC[C/T]GTCTCAAAAAAAAAA | 8208 |
rs370983918 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36394337 | GCCTCGGCCTCCCAA[A/G]GTGCTGGGATTACAG | 8208 |
rs371063655 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36407776 | TGAGGTCAGGAGTTC[A/G]AGACCACCCTGGCCA | 8208 |
rs371122870 | snp | A/G | 2.18931e-05 | 0.00330848 | utr-variant-3-prime | CHAF1B | GRCh38.p7 | 21:36416406 | CCTACCAGGCTCCCG[A/G]TGTGTGCAGGGAGAC | 8208 |
rs371237489 | in-del | -/TCA | | | upstream-variant-2KB, cds-indel | CHAF1B | GRCh38.p7 | 21:36384631 | AGCTGGCTAAAAGCA[-/TCA]GCCGGTATTTATATA | 8208 |
rs371289350 | snp | A/G/T | 8.23803e-05 | 0.00641749 | synonymous-codon | CHAF1B | GRCh38.p7 | 21:36402847 | ATCTTTGCTTCTCAC[A/G/T]CCAGGTGTGTTTCGT | 8208 |
rs371326990 | snp | C/G | | | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36378223 | ATACATGCACACATT[C/G]ATGTGTATGTATTTT | 8208 |
rs371344378 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36390862 | GGTCTTGCTCTCTTG[C/T]CCAGGCTGGTCTTGA | 8208 |
rs371404730 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36394568 | CTTAGAAGATGTGTA[C/T]GATATTTGCTGGGCA | 8208 |
rs371571594 | snp | A/G | 9.89332e-05 | 0.00703255 | intron-variant | CHAF1B | GRCh38.p7 | 21:36391707 | GTGATCTCTGTTTAC[A/G]ATGAGTGCATTAAAT | 8208 |
rs371708835 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36400121 | GGCGGAGGTCTTAGC[C/T]GTGAGCGGAGATCAT | 8208 |
rs371709051 | snp | G/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36410344 | TTACATTTGGGAAGT[G/T]TCAGCCATTTTTCCT | 8208 |
rs371925911 | snp | C/T | 7.32091e-05 | 0.00604973 | intron-variant | CHAF1B | GRCh38.p7 | 21:36413323 | ACACCCCGGTAAGAA[C/T]TTGTTGGAACAAGAT | 8208 |
rs372083852 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36393692 | CTCCCAACCTCAGGT[A/G]ATCCGCCCACCTCGG | 8208 |
rs372170568 | snp | C/T | 4.95593e-05 | 0.00497767 | intron-variant | CHAF1B | GRCh38.p7 | 21:36408735 | AGTGACTTTTCTTTC[C/T]TCTCCCTCCCTTCCC | 8208 |
rs372211386 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36393576 | CCTACCTCAGCCTCC[C/T]GAGTAGCTGGGATTA | 8208 |
rs372233313 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36408382 | TGGAATCCAGGAAAT[A/G]GAGATGAGGGTCCTA | 8208 |
rs372344270 | snp | C/G | 1.65192e-05 | 0.00287391 | missense, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36391556 | CACCCTGCAGATGCT[C/G]TCATCCTATTGTGGA | 8208 |
rs372352704 | snp | C/T | 0.000307953 | 0.0124049 | missense | CHAF1B | GRCh38.p7 | 21:36413213 | CCTTGCCGGGGCCTT[C/T]GGAGGAGAAGACCCT | 8208 |
rs372478630 | snp | C/T | 1.65269e-05 | 0.00287457 | utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36386114 | TGCCCGAGAAACGTT[C/T]TTCCCCTTCGAGACT | 8208 |
rs372512182 | snp | A/C/G | 0.000552625 | 0.0166137 | intron-variant | CHAF1B | GRCh38.p7 | 21:36402725 | TAGAAAACAAACAAA[A/C/G]AAAATAATAAAAATA | 8208 |
rs372577960 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36401866 | CTGCCTCAGCCTCCC[A/G]AGAAGCTGGGATTAC | 8208 |
rs372618016 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CHAF1B | GRCh38.p7 | 21:36398341 | TTACAGGTGTGCTAC[A/G]GTGATTTTTATTTTT | 8208 |
rs372652079 | snp | A/T | | | utr-variant-3-prime | MORC3 | GRCh38.p7 | 21:36376145 | GTCTTTCTCAAACAA[A/T]ACTACATACCTTTTA | 8208 |
rs372761555 | snp | A/C | 0.000153988 | 0.00877328 | missense, intron-variant | CHAF1B | GRCh38.p7 | 21:36397473 | AGGAGTAACCTGGGA[A/C]CCTTTGGGTCAATAT | 8208 |
rs372789572 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36399325 | ACAGGCGTGAGCTAC[C/T]GCGCCCGGCCTGTAA | 8208 |
rs372818231 | in-del | -/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36387821 | TTGAGCTGGATATGC[-/T]TTTTTTTTTTTTTTG | 8208 |
rs372828379 | snp | A/T | | | utr-variant-3-prime | CHAF1B | GRCh38.p7 | 21:36416701 | ACTTCATGGAGGGAC[A/T]CCTTTTCAATAAGAA | 8208 |
rs372837159 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | CHAF1B | GRCh38.p7 | 21:36395171 | TTCTCCTGCCTCAGC[A/G]TCCTGAGTAGCTGGA | 8208 |
rs372990450 | in-del | -/GAGTT | | | upstream-variant-2KB, intron-variant | CHAF1B | GRCh38.p7 | 21:36383469 | TTTTTTTTCGAAGCT[-/GAGTT]AAGAGTTAGTCCCTT | 8208 |
rs373001534 | snp | A/C/G | 0.000604218 | 0.0173724 | utr-variant-3-prime | MORC3 | GRCh38.p7 | 21:36375314 | TATATGTTATGTAAG[A/C/G]TAAAATATTTGCTCA | 8208 |
rs373045673 | snp | G/T | 1.65252e-05 | 0.00287443 | missense, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36386242 | AGACTGGCGTCTGCC[G/T]GCGTGGACACCAATG | 8208 |
rs373052760 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36403229 | TTGGGAGGCTGAGGC[A/G]GGCGGATCACTTGAG | 8208 |
rs373133195 | snp | A/G | 3.44382e-05 | 0.00414945 | splice-acceptor-variant | CHAF1B | GRCh38.p7 | 21:36416274 | TTTGTTAATGTTGCA[A/G]AGACGCCTGGAGACG | 8208 |
rs373223403 | snp | C/T | 0.000628598 | 0.0177173 | intron-variant | CHAF1B | GRCh38.p7 | 21:36409505 | GTTATGTTTTCTCTC[C/T]GAAACAGGTCACCAG | 8208 |
rs373243875 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36406565 | TGCTGGGATTACAGG[C/T]GTGAGCCACTGCACC | 8208 |
rs373289311 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | CHAF1B | GRCh38.p7 | 21:36387040 | TTTGATTCATTTTCC[C/G/T]TAGATTATTGTAACT | 8208 |
rs373317088 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36394690 | GCAGGAAGAAATATT[C/T]TAAGCATCTATAAAA | 8208 |
rs373321906 | snp | C/G/T | 0.000153988 | 0.00877328 | intron-variant | CHAF1B | GRCh38.p7 | 21:36386300 | ATCCGGGAACACTGC[C/G/T]TGAAGCAATAGTTTT | 8208 |
rs373421174 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36389680 | CAAAATAAAACAGAA[A/G]TCTAAAGTTTTTTTT | 8208 |
rs373503287 | snp | A/G/T | 0.00199481 | 0.0315187 | | | GRCh38.p7 | 21:36378128 | GGGAAGCAGAGCGGT[A/G/T]CCCCGGTAGAGATGT | 8208 |
rs373552914 | snp | A/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36382614 | GCATGATCTTGGCTC[A/T]CTGCCCTCTGGGTTC | 8208 |
rs373630889 | in-del | -/AAGCGATTCTC | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36395150 | CCACCTCCCGGGTTC[-/AAGCGATTCTC]CTGCCTCAGCATCCT | 8208 |
rs373695648 | snp | A/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36397655 | ATACTCATTCTTACA[A/T]CATAATCAGAAATTG | 8208 |
rs373729241 | snp | C/T | | | intron-variant, upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36380732 | GACCACAGGCACACA[C/T]CACTATGCCCAGCTA | 8208 |
rs373770332 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CHAF1B | GRCh38.p7 | 21:36401174 | CCGGTGGCTGAGGCA[C/T]GAGGATCACTGGAAC | 8208 |
rs373893737 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36399127 | GCAACCTCTGCCTCC[C/T]GGGTTCAAGTGATTC | 8208 |
rs373907249 | snp | C/T | 0.000214195 | 0.0103466 | synonymous-codon | CHAF1B | GRCh38.p7 | 21:36402784 | CCGGATGTTTCACGA[C/T]GACAGCATGAAGTCT | 8208 |
rs374028841 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36415546 | CCGGCTGCCTGTTTA[C/T]GCCTCAGCAGGGGGC | 8208 |
rs374056364 | snp | A/G | 0.000335944 | 0.012956 | synonymous-codon | MORC3 | GRCh38.p7 | 21:36375281 | TGAACAAATGAGTGA[A/G]ATCAGTAGTACTTAA | 8208 |
rs374110685 | in-del | -/T | 0.167484 | 0.23599 | intron-variant | CHAF1B | GRCh38.p7 | 21:36401574 | TATACATAATATATA[-/T]TTTTATATTATACAT | 8208 |
rs374133576 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36402290 | GCACTCTAGCCTGGG[C/T]GACAGAGCGAGACTC | 8208 |
rs374235160 | snp | C/T | | | intron-variant, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36381688 | GTGCATCACACACAT[C/T]CATGTTGCTGCCTGT | 8208 |
rs374268527 | snp | A/C/G | 0.000102744 | 0.00716683 | synonymous-codon | CHAF1B | GRCh38.p7 | 21:36413262 | CACAAAAGCCCACCC[A/C/G]TCCCGGAGGGTCACT | 8208 |
rs374395395 | snp | A/G | 6.59272e-05 | 0.00574101 | synonymous-codon, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36391651 | CAAGGAGAACTGGAC[A/G]GTTGTGAAGACTCTG | 8208 |
rs374622617 | snp | A/G | 6.77683e-05 | 0.00582061 | utr-variant-3-prime | CHAF1B | GRCh38.p7 | 21:36416412 | AGGCTCCCGGTGTGT[A/G]CAGGGAGACGGTAAA | 8208 |
rs374731467 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36406628 | ATTGTATGTAGTTGT[A/G]TATGACATGATGTTT | 8208 |
rs374758231 | snp | C/G | 0.000153988 | 0.00877328 | intron-variant | CHAF1B | GRCh38.p7 | 21:36387763 | TCAGAGATTCTTCGG[C/G]AACCAGATAGATACC | 8208 |
rs374791353 | snp | A/G | 0.00013229 | 0.0081319 | intron-variant | CHAF1B | GRCh38.p7 | 21:36402753 | ATAAATTTTGTGTGC[A/G]ACAGGCAAGAAGCTA | 8208 |
rs374870960 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36398470 | GTTCAAGCGATTCTC[C/T]TGCCTCATCCTCCTG | 8208 |
rs374984835 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | CHAF1B | GRCh38.p7 | 21:36399482 | GTGAAGCATAATTCA[C/T]TTACTAGAAGTGGTA | 8208 |
rs375101149 | snp | C/G/T | 9.95946e-05 | 0.00705615 | intron-variant | CHAF1B | GRCh38.p7 | 21:36386280 | AAACTGGGGCAGAGA[C/G/T]AGACATCCGGGAACA | 8208 |
rs375118597 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | CHAF1B | GRCh38.p7 | 21:36399278 | TGACCTCAAGTGATT[C/T]ACCCGCCTCTGCCTC | 8208 |
rs375151589 | snp | A/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36410594 | TTTCTTTGTTGTGGT[A/T]CTCATCTCTAGAGAT | 8208 |
rs375302132 | snp | A/G | 1.66308e-05 | 0.00288359 | missense | CHAF1B | GRCh38.p7 | 21:36415308 | AGGAGAATAAACTTA[A/G]CACCCTTAAAGACGG | 8208 |
rs375331531 | snp | A/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36391487 | AAAAAAAAATGAAAA[A/T]AAAAATCCTAATATG | 8208 |
rs375332094 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36404721 | TTATAGGTGTGAGCC[A/G]TTGCGCTGGCCTTTT | 8208 |
rs375351314 | snp | A/G | 6.95471e-05 | 0.0058965 | intron-variant | CHAF1B | GRCh38.p7 | 21:36412880 | CCCTGTTTTGGGGAC[A/G]AAGGTCCAGCGATGG | 8208 |
rs375376353 | snp | C/T | 1.64833e-05 | 0.00287078 | synonymous-codon, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36394577 | TGTGTATGATATTTG[C/T]TGGGCAACTGATGGG | 8208 |
rs375377025 | snp | G/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36379500 | CTCACTGAAGTGGCT[G/T]GAAAATCTAAATAGA | 8208 |
rs375381530 | snp | A/C | 9.92244e-05 | 0.00704289 | missense | CHAF1B | GRCh38.p7 | 21:36415366 | GTGTGATTTCCACCC[A/C]TTCTACAGAAGAAAT | 8208 |
rs375429611 | in-del | -/AG | 0.0166325 | 0.0896639 | intron-variant | CHAF1B | GRCh38.p7 | 21:36412385 | TTTTTTTTTTGAAAC[-/AG]AGTCTCACTGTCATC | 8208 |
rs375462922 | in-del | -/GGG | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36396331 | CATAAGTGTGATGGG[-/GGG]TTGTTACTGAACCTC | 8208 |
rs375522824 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36386778 | GAGTGCAGTGGTGCA[A/G]TCTCGACTTACTGCA | 8208 |
rs375539352 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon | CHAF1B | GRCh38.p7 | 21:36399524 | TTCTTTCTTCAGGGT[A/G]CTGCGAGTATACAGT | 8208 |
rs375564768 | snp | G/T | | | downstream-variant-500B | MORC3 | GRCh38.p7 | 21:36376829 | GTTTTCAAAAGCTTT[G/T]TCTCAGCCTGGCGCA | 8208 |
rs375623457 | snp | A/G | 1.65844e-05 | 0.00287957 | missense | MORC3 | GRCh38.p7 | 21:36375282 | GAACAAATGAGTGAA[A/G]TCAGTAGTACTTAAA | 8208 |
rs375670846 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | CHAF1B | GRCh38.p7 | 21:36388103 | GTTGGGATTACAGGC[G/T]TGAGCCACTGCGCCC | 8208 |
rs375752306 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36396594 | GGGAAGTTGAGGCTG[C/T]AGTGAGCTCTGACGG | 8208 |
rs375786228 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36401960 | TGGCCAGGCTGGTCT[C/T]GTACTCCTGGACTCA | 8208 |
rs375860533 | snp | A/G | 3.35503e-05 | 0.00409561 | missense | CHAF1B | GRCh38.p7 | 21:36413219 | CGGGGCCTTCGGAGG[A/G]GAAGACCCTGCAGCC | 8208 |
rs375927375 | snp | C/T | | | missense | CHAF1B | GRCh38.p7 | 21:36413081 | CGGTAGAGGGAACCC[C/T]TGCCAGCAGAACCCA | 8208 |
rs376013076 | snp | A/G | 1.65004e-05 | 0.00287227 | synonymous-codon | CHAF1B | GRCh38.p7 | 21:36413067 | GCCAGGACCCAGACC[A/G]GTAGAGGGAACCCCT | 8208 |
rs376014763 | snp | C/T | 0.000233279 | 0.0107975 | intron-variant | CHAF1B | GRCh38.p7 | 21:36391520 | GGAGTGTGGGTGAAG[C/T]GTGGATCACTGTTAC | 8208 |
rs376058259 | snp | C/G/T | 3.29654e-05 | 0.00405978 | synonymous-codon, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36386181 | GCACAACAAGGAGCC[C/G/T]GTGTACAGCCTGGAC | 8208 |
rs376106303 | in-del | -/A | 0.474 | 0.111014 | intron-variant | CHAF1B | GRCh38.p7 | 21:36391464 | GTGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 8208 |
rs376165251 | snp | A/G | 0.000216622 | 0.010405 | intron-variant | CHAF1B | GRCh38.p7 | 21:36394500 | CAGGGGTAAGCTGCT[A/G]TACCTGGGGAGTAAT | 8208 |
rs376201329 | snp | C/T | | | missense | CHAF1B | GRCh38.p7 | 21:36413093 | CCCCTGCCAGCAGAA[C/T]CCAAGACCCCAGCAG | 8208 |
rs376443251 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36400883 | TACTGGCTTCACACG[C/G]GGACATGGTGCAAAT | 8208 |
rs376476845 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36387699 | TGTGCGTTTTTCTCC[A/G]ACTGGGGAAATTTTA | 8208 |
rs376520302 | in-del | -/A | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36407991 | TCAAAGAAAAAAAAA[-/A]GAGGGCAGCTATGTA | 8208 |
rs376573502 | snp | A/G | 3.37336e-05 | 0.00410678 | missense | CHAF1B | GRCh38.p7 | 21:36416328 | AAGCGGCCCAGACTC[A/G]ATGAAAACAAAGGAG | 8208 |
rs376593479 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36405835 | GGAAAGATATGTCGT[A/G]TTCTAACAATTAACA | 8208 |
rs376600849 | in-del | -/G | 0.00318978 | 0.0398085 | upstream-variant-2KB, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36384363 | AAGCCCCTGGAGCAC[-/G]GGCCTCTGCTGGATA | 8208 |
rs376663242 | snp | G/T | | | utr-variant-3-prime | CHAF1B | GRCh38.p7 | 21:36416647 | TATCCAGTGTGAAAA[G/T]CAGTGAGTCCTCCCT | 8208 |
rs376882750 | snp | G/T | 3.30885e-05 | 0.00406733 | synonymous-codon | CHAF1B | GRCh38.p7 | 21:36412920 | GGCCATTTCTTCCAC[G/T]GACGGTTACTGCTCA | 8208 |
rs377006608 | in-del | -/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36401597 | TATACATAATATATA[-/T]TTTTATATTATACAT | 8208 |
rs377129652 | snp | A/G | | | downstream-variant-500B | MORC3 | GRCh38.p7 | 21:36376688 | AATTATTTTAAAACT[A/G]AAAATGTATTCATTA | 8208 |
rs377157345 | snp | G/T | 3.29511e-05 | 0.00405887 | intron-variant | CHAF1B | GRCh38.p7 | 21:36387744 | TGGTGAGTATTGCTG[G/T]CCTTCAGAGATTCTT | 8208 |
rs377170948 | snp | A/G | 1.6676e-05 | 0.00288751 | intron-variant | MORC3 | GRCh38.p7 | 21:36375129 | TCTAATAAGTTACAT[A/G]TTTGTATTTGCAGCC | 8208 |
rs377187130 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36391187 | GGTGATTTTGTATAG[C/T]TCTGATCTGTTATGA | 8208 |
rs377206785 | in-del | -/TTCT | | | intron-variant, upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36381108 | TTCTTTTTCTTCTTC[-/TTCT]TTTTTTTTTTTTTTT | 8208 |
rs377207071 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36382616 | ATGATCTTGGCTCAC[C/T]GCCCTCTGGGTTCAA | 8208 |
rs377214460 | snp | C/G | 0.000153988 | 0.00877328 | missense, intron-variant | CHAF1B | GRCh38.p7 | 21:36397496 | GTCAATATGTTGCTA[C/G]TCTGAGCTGTGACAG | 8208 |
rs377266252 | snp | A/C | 1.67758e-05 | 0.00289614 | missense | CHAF1B | GRCh38.p7 | 21:36416298 | GGAGACGCTCAGGGC[A/C]GTCCCCCAGAGCTAA | 8208 |
rs377324005 | snp | C/T | 1.6473e-05 | 0.00286988 | missense | CHAF1B | GRCh38.p7 | 21:36411525 | TCGGAGGATTCCGTG[C/T]TTCTGTATGACACCC | 8208 |
rs377413969 | in-del | -/GCGCGC/GCGCGCGC | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36389800 | TGTGTGTGTGTGTGT[-/GCGCGC/GCGCGCGC]GCGCGCGCACGCTGA | 8208 |
rs377457789 | in-del | -/AATA | | | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36378811 | ATGTACATTTAAATA[-/AATA]TTGCCATCCAAAAAA | 8208 |
rs377510748 | snp | A/G | 0.000193981 | 0.00984647 | intron-variant | CHAF1B | GRCh38.p7 | 21:36399469 | AAGTTGTTTCTGTGT[A/G]AAGCATAATTCATTT | 8208 |
rs377511926 | snp | C/T | 0.000477607 | 0.0154459 | utr-variant-3-prime | CHAF1B | GRCh38.p7 | 21:36416404 | AGCCTACCAGGCTCC[C/T]GGTGTGTGCAGGGAG | 8208 |
rs377525212 | snp | C/T | 0.0588605 | 0.161139 | intron-variant | CHAF1B | GRCh38.p7 | 21:36394973 | TAACCTCAGGTGATC[C/T]GCCCGCCTCAGCCTC | 8208 |
rs377536630 | snp | A/G | 1.65012e-05 | 0.00287234 | intron-variant | CHAF1B | GRCh38.p7 | 21:36409486 | CTCAGAGCCTCAGGG[A/G]TGTGTTATGTTTTCT | 8208 |
rs377637353 | snp | A/C | 0.00119737 | 0.0244387 | downstream-variant-500B | MORC3 | GRCh38.p7 | 21:36377000 | CATGCCTGTAATCCC[A/C]GCTACTCAGGAGGCT | 8208 |
rs377720200 | snp | G/T | 6.59794e-05 | 0.00574329 | intron-variant | CHAF1B | GRCh38.p7 | 21:36399487 | GCATAATTCATTTAC[G/T]AGAAGTGGTAAATCA | 8208 |
rs377724094 | snp | A/G | 4.12933e-05 | 0.00454367 | utr-variant-3-prime | CHAF1B | GRCh38.p7 | 21:36416394 | TTCTGCTCGAAGCCT[A/G]CCAGGCTCCCGGTGT | 8208 |
rs386818294 | in-del | AACCTCCGCCT/CC | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36382619 | ATCTTGGCTCACTGC[AACCTCCGCCT/CC]TCTGGGTTCAAGTGA | 8208 |
rs386818295 | multinucleotide-polymorphism | CT/TG | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36393836 | AATCTCATTTTAATG[CT/TG]TAGTTCTGGAGATTG | 8208 |
rs397749822 | in-del | -/T | 0.5 | 0 | intron-variant | CHAF1B | GRCh38.p7 | 21:36411131 | CTTTTTTTTTTTTTT[-/T]GTGACAGAGTCTTCC | 8208 |
rs397866513 | in-del | -/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36397294 | ACAGAGTCTCTCACT[-/T]ACTGCCTGCTGAGTG | 8208 |
rs397866716 | in-del | -/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36397740 | TTTTTTTTTTTTTTT[-/T]AGACACAGTCTCACT | 8208 |
rs397867015 | in-del | -/T | | | intron-variant, upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36381303 | TTTTTTTTTTTTTTT[-/T]CTAGATACGGAGTCT | 8208 |
rs397867346 | in-del | -/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36394430 | GCCAGGCTGGCCTTG[-/G]AACTCCTGACCACAG | 8208 |
rs398040601 | in-del | -/T | 0.464523 | 0.128375 | intron-variant | CHAF1B | GRCh38.p7 | 21:36382539 | TTTTCTTTTTCTTTC[-/T]TTTTTTTTTTTTTTT | 8208 |
rs398040602 | in-del | -/TAT | 0.5 | 0 | intron-variant | CHAF1B | GRCh38.p7 | 21:36382696 | ACCATGCCTGGCTGT[-/TAT]TATTATTATTATTAT | 8208 |
rs527349829 | snp | C/G | 0.00318978 | 0.0398085 | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36378610 | GAGGCAGGAGAATCA[C/G]TTAACCCCAGGAGGC | 8208 |
rs527429586 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36393002 | ATCACTCGCGATTAG[C/G]AGCTGGAGACCAGCC | 8208 |
rs527436687 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36385955 | TCAGATGGCAACGTT[A/T]ACATCCTTTCCCAAT | 8208 |
rs527449079 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36391308 | CTGAACAACATAAAT[A/G]TTGTTTTAATACCCT | 8208 |
rs527466075 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36392627 | GGGGCGGCTGCTGGG[C/T]GGAGGGGCTCCTCTC | 8208 |
rs527561020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36414339 | CTCAGCCTCTCCTGC[A/G]CCAATAGGTCTTCTT | 8208 |
rs527588555 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36398203 | GACTACGGGTGTGCA[C/T]CACCACACCCGGCTA | 8208 |
rs527640470 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36396847 | GTGACCCTCTTTGTC[A/G]TCTTCTAAACCTGTT | 8208 |
rs527679698 | snp | A/G | 0 | 0 | intron-variant | CHAF1B | GRCh38.p7 | 21:36404716 | TGGGATTATAGGTGT[A/G]AGCCATTGCGCTGGC | 8208 |
rs527706373 | snp | A/G | | | utr-variant-3-prime | MORC3 | GRCh38.p7 | 21:36375835 | TTCCTGTCCTGAAAT[A/G]TTTTATTCATGAAAA | 8208 |
rs527715934 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CHAF1B | GRCh38.p7 | 21:36412229 | CCCTCTGGGAGGAAG[C/T]CCTTCCCTGCATGCC | 8208 |
rs527810632 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CHAF1B | GRCh38.p7 | 21:36411783 | ACCCGGGCTGGAGTG[C/T]AGTGGTGTGATCTCG | 8208 |
rs527829785 | snp | C/G | 0 | 0 | intron-variant | CHAF1B | GRCh38.p7 | 21:36394966 | AAACTCCTAACCTCA[C/G]GTGATCTGCCCGCCT | 8208 |
rs527831169 | snp | A/C | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 21:36377781 | GACGCTTGATTCTTG[A/C]TGTCACATGAGACGT | 8208 |
rs527935953 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | CHAF1B | GRCh38.p7 | 21:36383759 | GTTCACGCCATTGTC[C/T]TGCCTCAGCCTCCCG | 8208 |
rs528036557 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36391492 | AAAATGAAAATAAAA[A/G]TCCTAATATGAAGGA | 8208 |
rs528044901 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36408884 | TTTTAGACGGAGTTT[C/T]GCTCTTGTTGCCCAG | 8208 |
rs528048564 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36382916 | TTTCACCATGTTGGC[C/T]AGGCTGGTCTCAAAT | 8208 |
rs528090128 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36401564 | ATTTTTATATTATAC[A/G]TAATATATATTTTTA | 8208 |
rs528096980 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant | CHAF1B | GRCh38.p7 | 21:36385426 | GCGGGAGGTGACGGT[A/G]CCTCTGACTGTCCGG | 8208 |
rs528127641 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36409605 | TTTTAAAAATATTTT[A/C]TTTTTACATTTAAAT | 8208 |
rs528235160 | snp | A/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36406495 | TTTACCATGTTGGCC[A/T]GGGTGGTCTCAAACT | 8208 |
rs528291015 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36381271 | GACTATAGGTGCATG[C/T]CACCATGCCTGGCTG | 8208 |
rs528436854 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CHAF1B | GRCh38.p7 | 21:36388663 | GTAGAGATGGGGTTT[C/T]GCCTTGTCAGCCAGG | 8208 |
rs528479037 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CHAF1B | GRCh38.p7 | 21:36394304 | ATGGTCTCGATCTCC[C/T]GACCTTGTGATCTGC | 8208 |
rs528548378 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36400631 | GGAAGATCCCTACAC[A/G]AGGCAACAGAAGACA | 8208 |
rs528643607 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36404455 | TTTATTTATTTTGAG[A/T]TGGAGTTTCGCTCTT | 8208 |
rs528675863 | snp | C/G | 1.6495e-05 | 0.0028718 | intron-variant | CHAF1B | GRCh38.p7 | 21:36399489 | ATAATTCATTTACTA[C/G]AAGTGGTAAATCAGA | 8208 |
rs528684916 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36408166 | CAGTGTATGATGGTC[A/G]CTCTGACAGGGCTGA | 8208 |
rs528871970 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CHAF1B | GRCh38.p7 | 21:36383797 | GGGACTACAGGCGCC[C/T]GCCGCCACGCCCGAC | 8208 |
rs528957057 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | CHAF1B | GRCh38.p7 | 21:36397985 | TGCCTGCCTTGGCCA[A/C]TGTGCTGGGATTACA | 8208 |
rs528972595 | snp | C/T | 0.000214378 | 0.010351 | missense, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36391605 | AGCCGGAGCAGATCG[C/T]TTTTCAGGATGAGGA | 8208 |
rs529088259 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36411666 | GTATCCTGGAAGACA[C/T]CCCGGGGTTAGGGAG | 8208 |
rs529112006 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36403228 | TTTGGGAGGCTGAGG[C/T]GGGCGGATCACTTGA | 8208 |
rs529166046 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CHAF1B | GRCh38.p7 | 21:36411217 | CTCCTGGGTTCAAGC[A/G]ATTCTCCTGTCTCAG | 8208 |
rs529284735 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | MORC3 | GRCh38.p7 | 21:36376620 | TAATAAAATAAAAAT[A/G]TATGATGGCTAACTG | 8208 |
rs529394391 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36390885 | GGTCTTGAGCTCCTG[G/T]GCTAAAACAACCCTT | 8208 |
rs529404289 | snp | G/T | | | intron-variant, upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36380477 | TGTTTTTTTAGTTTT[G/T]TTTCCCCAGGCTGGT | 8208 |
rs529448734 | in-del | -/TTT | 0.00119737 | 0.0244387 | intron-variant | CHAF1B | GRCh38.p7 | 21:36394377 | ACAGCACCTGGCTGA[-/TTT]TTGTATTTTGAGTAG | 8208 |
rs529777591 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36387852 | AGATAGAGTTTCACT[C/T]TTGTTCCCCAGGCTG | 8208 |
rs529777733 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36379306 | CGTGCACCACCATGC[C/G]CAGCTAATTTTTCTA | 8208 |
rs529812113 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36413408 | GTGAAATTTCAGGCG[A/G]TGAATGCTTCATGCC | 8208 |
rs529847534 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36386395 | TGGGAGGCTGAGGTG[A/G]GAGGATCGCTTGAGT | 8208 |
rs529947089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36392692 | CCTCACTTCTCAGAC[A/G]GGGCGGCCGGGCAGA | 8208 |
rs529963637 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36393030 | GCCCGGCCAACACAG[C/T]GAAACCCCATCTCCA | 8208 |
rs529968083 | snp | C/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36400654 | AGAAGACAGGCAGGT[C/T]GAGCGTTGGATCTGT | 8208 |
rs530031411 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | CHAF1B | GRCh38.p7 | 21:36398896 | CTTGGAATAAAAGTG[G/T]TAGGGAGGAGTTAGT | 8208 |
rs530119966 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36394408 | AGAGATGGGATTTTA[C/T]TGTGTTAGCCAGGCT | 8208 |
rs530185892 | snp | A/T | | | downstream-variant-500B | CHAF1B | GRCh38.p7 | 21:36416950 | TCGTTAATGTTGTAG[A/T]ATATTTCCTTAGCAT | 8208 |
rs530232750 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36412740 | CTGCATGAGTGAGTC[G/T]CTATCACACACTCTT | 8208 |
rs530280972 | snp | A/C | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 21:36377841 | ATCATTTAAGTTCTC[A/C]CCTCTGGCTGCGTAG | 8208 |
rs530331955 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36378491 | ATGAGGTCAGGAGAT[C/T]GAGACCATCCTGGCC | 8208 |
rs530438028 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36381068 | ATCTAGGCACAGATA[G/T]AGTCATTGTTTCTAG | 8208 |
rs530506949 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36402910 | GGGATGTCTGCTCCC[A/G]TTTTACGCTGCAGCT | 8208 |
rs530517038 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36396149 | GGATTACAGGCGCCC[A/G]CCACCACTCCCAGCT | 8208 |
rs530877634 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36381388 | TCAGCCTCCCAAAAT[G/T]TTGATATTACCGGCA | 8208 |
rs531122662 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36408336 | GAAGTTGGGGAAAGG[C/T]GAGTCTCAGCCTTTG | 8208 |
rs531123744 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | CHAF1B | GRCh38.p7 | 21:36400668 | TCGAGCGTTGGATCT[C/G]TCTGGCAGCAGGCAG | 8208 |
rs531213370 | snp | G/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36389965 | GCACGTGGAGAGTGT[G/T]CATCCATCAGGGCCA | 8208 |
rs531309888 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36392180 | AGCACATCTTGTACC[A/G]TCCTTAATCCATTTA | 8208 |
rs531316774 | snp | G/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 21:36377924 | TTAATTAAGTCAGCG[G/T]CCTTGGGGTTAGACC | 8208 |
rs531401247 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | CHAF1B | GRCh38.p7 | 21:36392583 | GGACGGGGCAGCTGC[C/T]GGGCAGAGATGCTCC | 8208 |
rs531432835 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | CHAF1B | GRCh38.p7 | 21:36404583 | GGGATTACAGGCATG[A/C]GCCACCACGCCCAGC | 8208 |
rs531468153 | in-del | -/AT | 0.0345262 | 0.126772 | intron-variant | CHAF1B | GRCh38.p7 | 21:36401423 | TTTATATTATACATA[-/AT]ATATATTTTTATATT | 8208 |
rs531561807 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36411761 | TGAGACCAAGTATCA[C/T]TCTGTCACCCGGGCT | 8208 |
rs531738845 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | MORC3 | GRCh38.p7 | 21:36376696 | TAAAACTAAAAATGT[A/G]TTCATTAGACCCTCA | 8208 |
rs531774301 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36383201 | TCAATGGATTCTCTT[G/T]CCTCAGCCTCCCTAG | 8208 |
rs531809271 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | CHAF1B | GRCh38.p7 | 21:36416541 | TATGGATGCTGTTGT[A/G]TTCAGTATCCATTTT | 8208 |
rs531870127 | snp | A/G | | | utr-variant-3-prime | MORC3 | GRCh38.p7 | 21:36376274 | CCCATGTTTTGTGCA[A/G]TTTTAAAGAGATGGC | 8208 |
rs531874805 | snp | C/G | | | upstream-variant-2KB, utr-variant-5-prime | CHAF1B | GRCh38.p7 | 21:36384543 | TCCTGTAGAAATCAG[C/G]CTTCAAGGAGCATAC | 8208 |
rs531875530 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36390962 | CACCCTGCCTATTAT[C/T]CCCATTTACAGGTGA | 8208 |
rs531913669 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHAF1B | GRCh38.p7 | 21:36396611 | GTGAGCTCTGACGGC[A/G]CCACTGCACTCCAGC | 8208 |
rs532121506 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36380648 | TAGCAGTGGCGCGAT[C/T]ACAGCTCACTACAGC | 8208 |
rs532130064 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36408910 | CCCAGGCTGGAGTGC[A/C]ATGGTGCGATCTCTG | 8208 |
rs532158652 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36379967 | TCACAGTTCACTGCA[C/G]CCTCAACCTCTCAGG | 8208 |
rs532367751 | snp | A/G | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36409745 | TCAAGTGATCCACCT[A/G]CCTCGGCCTCCCAAA | 8208 |
rs532394484 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36393057 | TCCACCAAAAAAATA[C/T]GAAAACCAGACAGGC | 8208 |
rs532541754 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36399945 | GCACTTTGGGAGACT[G/T]AGGTGGGCGGATCAC | 8208 |
rs532582300 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36399393 | TACCCAGTTGTGAAT[A/C]TCATTGGTAAAAGCT | 8208 |
rs532763346 | snp | A/C | | | | | GRCh38.p7 | 21:36378090 | ATATCCACTTTCTCA[A/C]TGGGGCAAGCAGGGG | 8208 |
rs532784461 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CHAF1B | GRCh38.p7 | 21:36399711 | CTGGCCACAAAGAGC[C/T]GATTCCAGAACTACA | 8208 |
rs532877701 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36399327 | AGGCGTGAGCTACCG[C/G]GCCCGGCCTGTAATA | 8208 |
rs532894415 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CHAF1B | GRCh38.p7 | 21:36402977 | CCGACTTACCTGCCC[A/G]TTGGAACCTCCAGGA | 8208 |
rs532903699 | snp | A/C | 0 | 0 | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36378534 | CCCCATCTCTACTAA[A/C]AATACAAAAATTAGC | 8208 |
rs532939810 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36397286 | GTTTTAGTACAGAGT[C/T]TCTCACTTACTGCCT | 8208 |
rs532995952 | snp | C/T | 3.37109e-05 | 0.0041054 | synonymous-codon | CHAF1B | GRCh38.p7 | 21:36416327 | AAAGCGGCCCAGACT[C/T]GATGAAAACAAAGGA | 8208 |
rs533031065 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | CHAF1B | GRCh38.p7 | 21:36379767 | AAGACAGAATAAATT[G/T]AAATTTGAATATAAA | 8208 |
rs533081749 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36415941 | TATTTTTAGTAGAGT[C/T]GGGGGTTTCACCACG | 8208 |
rs533154999 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36382314 | TTTGGGGCTATTATG[G/T]ATAATGATTCTTGTA | 8208 |
rs533185141 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36410386 | TTCTGTTATTCCCTT[C/T]TCTTATTCAAATACT | 8208 |
rs533238737 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36390071 | GGGTGCGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 8208 |
rs533343325 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36395026 | ATGAACCACTGCCCC[C/T]GGCCCTAACTTACCT | 8208 |
rs533377910 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | CHAF1B | GRCh38.p7 | 21:36401322 | ATATATAATATATAC[G/T]TTAATATGTTATATA | 8208 |
rs533473285 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36409291 | TAGGTGTGAGCCACC[A/G]CGCCCTGCCAAAATG | 8208 |
rs533474070 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | CHAF1B | GRCh38.p7 | 21:36389612 | TCTGTCTCAAAAAAA[A/T]AAAAAAAAAGTAAAC | 8208 |
rs533812525 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | CHAF1B | GRCh38.p7 | 21:36383926 | GTGCTGGGATTACAG[C/G]CGTGAGCTACCGCGA | 8208 |
rs533844628 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36391783 | TCTCATTGTCGCCCA[G/T]GCTGGAGTGCTGTAC | 8208 |
rs533929500 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 21:36378126 | AGGGGAAGCAGAGCG[A/G]TGCCCCGGTAGAGAT | 8208 |
rs533930034 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36391311 | AACAACATAAATGTT[A/G]TTTTAATACCCTAAA | 8208 |
rs533967313 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36397015 | ACCTCTCCCTGCTCC[A/C]TATTCACTTCGCTAA | 8208 |
rs534094450 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36411369 | TCCACCCGGCTCGGC[C/T]TCCCAAAGTGCTGGG | 8208 |
rs534234307 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | CHAF1B | GRCh38.p7 | 21:36404043 | GTAGTTGTTTAGGTT[A/G]TATTTACTAAAGTTA | 8208 |
rs534268094 | snp | G/T | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36393394 | GATTTTCTTAGTTTC[G/T]GCTATACATTTTTCT | 8208 |
rs534317690 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CHAF1B | GRCh38.p7 | 21:36394468 | GTCTACCTTGGCCTC[C/T]CAAAGTGCTGGGATT | 8208 |
rs534352735 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CHAF1B | GRCh38.p7 | 21:36394175 | TCTGCCTCCCAGGTT[C/G]AAGTGATTCCCCTCC | 8208 |
rs534427572 | in-del | -/TT | | | intron-variant | CHAF1B | GRCh38.p7 | 21:36404733 | GCCATTGCGCTGGCC[-/TT]TTTTTTTTTTTTTTT | 8208 |