chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5159590044159590045CT28GENIChomozygous964016452
5159590355159590356AC29GENIChomozygous964016453
5159590356159590357GC29GENIChomozygous964016454
5159590377159590378GA32GENIChomozygous964016455
5159590516159590517AG25GENIChomozygous964016456
5159590543159590544TC24GENIChomozygous964016457
5159590567159590568TC25GENIChomozygous964016458
5159590810159590811GA32GENIChomozygous964016459
5159591041159591042CT23GENIChomozygous964016460
5159591165159591166AG27GENIChomozygous964016461
5159591294159591295GA30GENIChomozygous964016462
5159591492159591493CT31GENIChomozygous964016463
5159591711159591712GA36GENIChomozygous964016464
5159591959159591960CT23GENIChomozygous964016465
5159592241159592242AG32GENIChomozygous964016466
5159592551159592552GA38GENIChomozygous964016467
5159592593159592594GA46GENIChomozygous964016468
5159592713159592714CT34GENIChomozygous964016469
5159593011159593012TA27GENIChomozygous964016470
5159593229159593230AG54GENIChomozygous964016471
5159593316159593317AC43GENIChomozygous964016472
5159594481159594482GA39GENIChomozygous964016473
5159595521159595522GA32GENIChomozygous964016474
5159598268159598269GA32GENIChomozygous964016475
5159599504159599505TC30GENIChomozygous964016476
5159600471159600472TC28GENIChomozygous964016477
5159601143159601144CT44GENIChomozygous964016478
5159601217159601218AG41GENIChomozygous964016479
5159601274159601275AG28GENIChomozygous964016480
5159602018159602019CT6GENIChomozygous964016481