chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71795546217955463TC6GENIChomozygous138023744
71795675417956755A15GENIChomozygous137939270
71795692117956922AG22GENIChomozygous138023745
71795695917956960AC21GENICpossibly homozygous138023746
71795699117956992GT18GENIChomozygous138023747
71796203317962034TA21GENIChomozygous138023748
71796204317962044AC22GENIChomozygous138023749
71796204417962045TG22GENIChomozygous138023750
71796204617962047GT23GENIChomozygous138023751
71796241717962418AT24GENIChomozygous138023752
71796277217962773TC23GENIChomozygous138023753
71796280917962810G24GENIChomozygous137939271
71796500117965001AT25GENIChomozygous137939272
71796633717966337G18GENIChomozygous137939273
71796750117967502AG16GENIChomozygous138023754
71796839217968393AG27GENIChomozygous138023755
71796858117968582GA15GENIChomozygous138023756
71797033717970338TC22GENIChomozygous138023757
71797445117974452GA17GENIChomozygous138023758
71797515917975160TC17GENIChomozygous138023759
71797536817975368TG25GENIChomozygous137939274
71797675417976755GA14GENIChomozygous138023760
71797677717976778CT12GENIChomozygous138023761
71797777017977770GTG21GENIChomozygous137939275
71797848917978489CAG20GENIChomozygous137939276
71797882917978830TC20GENIChomozygous138023762