chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X65570176557018TA20GENIChomozygous108219743
X65583016558302CG17GENIChomozygous108219745
X65590896559090GA10GENIChomozygous108219747
X65625396562539A13GENIChomozygous129717661
X65626296562630AT20GENIChomozygous108219749
X65664316566432TC11GENIChomozygous108219751
X65709676570967C15GENIChomozygous129717662
X65712156571216AG6GENIChomozygous108219753
X65731626573162T7GENIChomozygous129717663
X65731656573165T7GENIChomozygous129717664
X65771936577194AT12GENIChomozygous108219755
X65775706577571AT18GENIChomozygous108219757
X65784426578443AT13GENIChomozygous108219759
X65793426579347GTATG17GENIChomozygous129717666
X65831616583169CTAGCTAG8GENICheterozygous131239033
X65831846583185G8GENICpossibly homozygous129717667
X65831866583189TAG8GENICpossibly homozygous129717668
X65854936585494A7GENIChomozygous129717669
X65859266585927TA11GENICheterozygous120526634
X65859306585931AG12GENICheterozygous120526635
X65730526573053AG4GENIChomozygous119983717
X65859346585935GA12GENICheterozygous120526636
X65859356585936TG12GENICheterozygous120526637
X65856216585622TC7GENIChomozygous119901820
X65893066589307GA18GENIChomozygous108219761
X65894556589456T11GENIChomozygous129717670
X65985396598540CT11GENIChomozygous108219763
X66022776602278GT17GENIChomozygous108219765
X66022836602284GT17GENIChomozygous108219767
X66022876602288T18GENIChomozygous129717673
X66072516607252C9GENIChomozygous129717674
X66152626615263T13GENIChomozygous129717676
X65889176588918GA2GENICheterozygous134258873