chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7123963136123963137GT13GENIChomozygous54091558
7123963294123963295AT17GENIChomozygous54091560
7123965962123965963CT29GENIChomozygous54091562
7123966166123966167GA29GENIChomozygous54091564
7123966714123966715AG25GENIChomozygous54091566
7123968071123968072TC28GENIChomozygous54091567
7123968092123968093GA31GENIChomozygous54091569
7123968614123968615CT33GENIChomozygous54091571
7123968675123968676GA31GENIChomozygous54091573
7123969622123969623TC31GENIChomozygous54091575
7123969895123969896CA21GENIChomozygous54091577
7123971180123971181T-15GENICpossibly homozygous54091580
7123972384123972385CT47GENIChomozygous54091582
7123972491123972492AG41GENIChomozygous54091584
7123972517123972518TC31GENIChomozygous54091586
7123972571123972572CT36GENIChomozygous54091587