chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
85787880557878806GGA28GENIChomozygous52656875
85787923857879239GA22GENIChomozygous52656877
85788101557881016CT19GENIChomozygous52656883
85788130457881305C-19GENIChomozygous52656885
85788313157883132TC32GENIChomozygous52656887
85788395157883952CCA30GENIChomozygous52656889
85788537257885373TC31GENIChomozygous52656891
85788595457885955CT21GENIChomozygous52656893
85788917457889175TC27GENICpossibly homozygous52656895
85789115957891160AG27GENIChomozygous52656897
85789216357892164TTACACACACACACACACACACACAC6GENICheterozygous53576201
85789216357892164TTACACACACACACACAC6GENICheterozygous53432426
85789216357892164TTACACACACACACACACAC6GENICheterozygous53461147
85789247357892474GA21GENIChomozygous52656901
85789258857892589CT22GENIChomozygous52656903
85789276857892769GA31GENICpossibly homozygous52656905
85789331357893314GA25GENIChomozygous52656907
85789402657894027CA32GENIChomozygous53742359
85789457757894578AC11GENIChomozygous52656909