chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
465216566521657GA18GENIChomozygous113076504
465216786521679TC16GENIChomozygous113076505
465218246521825AG30GENIChomozygous113076506
465218756521876GA31GENIChomozygous113076507
465223586522359TC20GENIChomozygous112479421
465224006522401CT26GENIChomozygous113076508
465225416522542GA28GENIChomozygous113076509
465225836522584TC24GENIChomozygous113076510
465228826522883TC26GENIChomozygous112479425
465233676523368AG26GENIChomozygous113076511
465234166523417CT28GENIChomozygous112479427
465235346523535TC26GENIChomozygous112479429
465236866523687TC26GENIChomozygous113076512
465239006523901CT22GENIChomozygous113076513
465247326524733AG14GENIChomozygous112479435
465248466524847TC27GENIChomozygous112479437
465250986525099CT28GENIChomozygous112479441
465251046525105GA26GENIChomozygous112479443
465251056525106CA26GENIChomozygous113076514
465253196525320TC26GENIChomozygous112479445
465255156525516AG20GENIChomozygous112479447
465257606525761CT8GENIChomozygous113076515
465261266526127TC4GENIChomozygous112479450
465265736526574TC17GENIChomozygous112479454
465265936526594GA14GENIChomozygous112479456
465268146526815AG20GENIChomozygous112479462
465269826526983GC16GENIChomozygous113076516
465270126527013CT16GENIChomozygous113076517
465272246527225AG18GENIChomozygous112479464
465276076527608TA20GENIChomozygous112479466
465276136527614CT37GENICheterozygous112479468
465288136528814CT16GENIChomozygous112479486
465276256527626GT36GENICheterozygous112479472
465276446527645TC40GENICheterozygous112479474
465276486527649CT33GENICheterozygous112479476
465289666528967GA20GENIChomozygous112479488
465293586529359AG15GENIChomozygous112479490
465298536529854TC12GENIChomozygous112479496
465298626529863CT11GENIChomozygous112479498
465298926529893TC15GENIChomozygous112479500
465299896529990CT23GENIChomozygous112479502