chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
85014046950140470GA31GENIChomozygous116815382
85014091950140920AT58GENICpossibly homozygous116815384
85014163750141638AG50GENIChomozygous116815386
85014428250144283CT54GENIChomozygous116815388
85014583150145832TG32GENIChomozygous116815390
85014590450145905AG55GENIChomozygous116815392
85014725250147253CT68GENIChomozygous116815394
85014787050147871AG53GENICpossibly homozygous116815396
85015135050151351GA65GENICpossibly homozygous116815398
85015155850151559CT51GENIChomozygous116815400
85015194950151950CA49GENIChomozygous116815402
85015195550151956CG47GENIChomozygous116815404
85015320150153202TG36GENIChomozygous116815406
85015320450153205AG32GENIChomozygous116815408
85015320750153208GA32GENIChomozygous116815410
85015322350153224CT25GENIChomozygous116815412
85015361150153612GA39GENICpossibly homozygous116815414
85015397850153979GA49GENIChomozygous116815416
85015482450154825AG54GENIChomozygous116815418
85015631450156315AG55GENIChomozygous116815420
85015832550158326TC50GENIChomozygous116815422
85015906650159067GA43GENIChomozygous116815424
85015919650159197GC39GENIChomozygous116815426
85015931850159319CT50GENIChomozygous116815428
85016003750160038CT70GENIChomozygous116815430