chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X123900994123900995AG22GENIChomozygous810304643
X123901333123901334TC17GENIChomozygous810304644
X123901666123901667CA27GENIChomozygous810304645
X123901786123901787CG14GENIChomozygous810304646
X123902364123902365TC13GENIChomozygous810304647
X123902771123902772CT33GENIChomozygous810304648
X123903040123903041CT23GENICpossibly homozygous810304649
X123903719123903720TA32GENIChomozygous810304650
X123904966123904967GA21GENIChomozygous810304651
X123905627123905628AG30GENIChomozygous810304652
X123906352123906353GT23GENIChomozygous810304653
X123906932123906933TA18GENIChomozygous810304654
X123907599123907600CT28GENICpossibly homozygous810304655
X123907796123907797CT23GENIChomozygous810304656
X123907829123907830TC18GENIChomozygous810304657
X123908139123908140AG48GENICheterozygous810304658
X123909136123909137CG21GENIChomozygous810304659
X123910070123910071TG39GENICpossibly homozygous810304660
X123910074123910075GA38GENIChomozygous810304661
X123910082123910083AG31GENIChomozygous810304662
X123910759123910760AC6GENIChomozygous810304663
X123910765123910766TG6GENIChomozygous810304664
X123910855123910856CT10GENIChomozygous810304665
X123910914123910915TA17GENIChomozygous810304666
X123911112123911113GT11GENIChomozygous810304667
X123911193123911194AT14GENIChomozygous810304668
X123911321123911322TC23GENIChomozygous810304669
X123911461123911462GT17GENIChomozygous810304670
X123912197123912198TC32GENIChomozygous810304671
X123914613123914614AG24GENIChomozygous810304672
X123916196123916197AG20GENIChomozygous810304673
X123916552123916553GA21GENIChomozygous810304674
X123916936123916937AG19GENIChomozygous810304675