chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5159590044159590045CT40GENIChomozygous775473489
5159590355159590356AC44GENIChomozygous775473490
5159590356159590357GC43GENIChomozygous775473491
5159590377159590378GA53GENIChomozygous775473492
5159590516159590517AG43GENIChomozygous775473493
5159590543159590544TC39GENIChomozygous775473494
5159590567159590568TC46GENIChomozygous775473495
5159590810159590811GA46GENIChomozygous775473496
5159590979159590980AG51GENICheterozygous775473497
5159591041159591042CT49GENIChomozygous775473498
5159591165159591166AG56GENIChomozygous775473499
5159591294159591295GA48GENIChomozygous775473500
5159591492159591493CT34GENIChomozygous775473501
5159591711159591712GA54GENIChomozygous775473502
5159591959159591960CT52GENIChomozygous775473503
5159592241159592242AG40GENIChomozygous775473504
5159592551159592552GA53GENIChomozygous775473505
5159592593159592594GA55GENIChomozygous775473506
5159592713159592714CT73GENIChomozygous775473507
5159593011159593012TA41GENIChomozygous775473508
5159593229159593230AG79GENIChomozygous775473509
5159593316159593317AC61GENICpossibly homozygous775473510
5159594481159594482GA45GENIChomozygous775473511
5159595521159595522GA62GENIChomozygous775473512
5159598268159598269GA56GENIChomozygous775473513
5159599504159599505TC51GENIChomozygous775473514
5159600471159600472TC40GENICpossibly homozygous775473515
5159601143159601144CT52GENIChomozygous775473516
5159601217159601218AG32GENIChomozygous775473517
5159601274159601275AG39GENIChomozygous775473518
5159602018159602019CT26GENICpossibly homozygous775473519