chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7123963136123963137GT36GENIChomozygous54091558
7123963294123963295AT19GENIChomozygous54091560
7123965962123965963CT28GENIChomozygous54091562
7123966166123966167GA30GENIChomozygous54091564
7123966714123966715AG27GENIChomozygous54091566
7123968071123968072TC49GENIChomozygous54091567
7123968092123968093GA42GENIChomozygous54091569
7123968614123968615CT13GENIChomozygous54091571
7123968675123968676GA19GENIChomozygous54091573
7123969622123969623TC23GENIChomozygous54091575
7123969895123969896CA27GENIChomozygous54091577
7123971036123971038AT--11GENIChomozygous54091578
7123971180123971181T-17GENICpossibly homozygous54091580
7123972384123972385CT32GENIChomozygous54091582
7123972491123972492AG24GENIChomozygous54091584
7123972517123972518TC27GENIChomozygous54091586
7123972571123972572CT27GENIChomozygous54091587