chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3107979922107979922C40GENIChomozygous136582630
3107980526107980527CT53GENIChomozygous136784593
3107982308107982309TC59GENIChomozygous136784594
3107982348107982349AG65GENIChomozygous136784595
3107982990107982991GC62GENIChomozygous136784596
3107983165107983166CT57GENIChomozygous136784597
3107983662107983663CT37GENIChomozygous136784598
3107983733107983734CT55GENIChomozygous136784599
3107984090107984090C52GENIChomozygous136582631
3107984375107984376GA44GENIChomozygous136784600
3107985758107985758G36GENIChomozygous136582632
3107987220107987221TC43GENIChomozygous136784601
3107987592107987593GA56GENIChomozygous136784602
3107988213107988214CA59GENIChomozygous136784603
3107988502107988503AG47GENIChomozygous136784604
3107989099107989100AG54GENIChomozygous136784605
3107989174107989175A47GENIChomozygous136582633
3107989721107989722AG55GENIChomozygous136784606
3107990218107990219TC55GENIChomozygous136784607
3107991367107991368A63GENIChomozygous136582634
3107992196107992197AT56GENICpossibly homozygous136784608
3107992698107992699CT49GENIChomozygous136784609
3107993684107993685CT58GENIChomozygous136784610
3107994174107994175GC37GENIChomozygous136784611
3107996009107996010GT43GENIChomozygous136784612
3107996035107996036CT54GENIChomozygous136784613
3107996126107996127TC69GENIChomozygous136784614
3107996184107996185GA68GENIChomozygous136784615
3107996414107996415TC57GENIChomozygous136784616
3107996902107996903CT44GENIChomozygous136784617
3107997015107997016CT39GENIChomozygous136784618
3107997077107997078CT38GENIChomozygous136784619
3107985763107985764G40GENICheterozygous145204564
3107985763107985764GA40GENIChomozygous403073262
3107997512107997513CT54GENIChomozygous136784620
3107997876107997877AG55GENIChomozygous136784621