chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
158552435085524351TC12GENIChomozygous887756675
158552439585524396TC18GENICpossibly homozygous887756676
158552493585524936AG11GENIChomozygous887756677
158552763985527640TG14GENIChomozygous887756678
158552788685527887AG16GENIChomozygous887756679
158552940185529402GT13GENIChomozygous887756680
158552940585529406AG14GENIChomozygous887756681