chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71795546217955463TC19GENIChomozygous138023744
71795675417956755A54GENIChomozygous137939270
71795692117956922AG61GENIChomozygous138023745
71795695917956960AC68GENIChomozygous138023746
71795699117956992GT62GENIChomozygous138023747
71796203317962034TA62GENIChomozygous138023748
71796204317962044AC60GENIChomozygous138023749
71796204417962045TG59GENIChomozygous138023750
71796204617962047GT61GENIChomozygous138023751
71796241717962418AT64GENIChomozygous138023752
71796277217962773TC63GENIChomozygous138023753
71796280917962810G69GENIChomozygous137939271
71796500117965001AT58GENIChomozygous137939272
71796633717966337G62GENIChomozygous137939273
71796750117967502AG41GENIChomozygous138023754
71796839217968393AG54GENIChomozygous138023755
71796858117968582GA44GENIChomozygous138023756
71797033717970338TC64GENIChomozygous138023757
71797445117974452GA48GENIChomozygous138023758
71797515917975160TC52GENIChomozygous138023759
71797536817975368TG51GENIChomozygous137939274
71797675417976755GA41GENICpossibly homozygous138023760
71797677717976778CT45GENICpossibly homozygous138023761
71797777017977770GTG36GENIChomozygous137939275
71797848917978489CAG53GENIChomozygous137939276
71797882917978830TC48GENIChomozygous138023762
71797895017978951TC59GENIChomozygous138023763
71797917717979178TC83GENIChomozygous138023764
71798009917980100T51GENICpossibly homozygous403202630
71798009917980100TA51GENICheterozygous154427166