chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1245478671245478672CT27GENIChomozygous992747460
1245480598245480599AT29GENICpossibly homozygous992747461
1245480625245480626CT29GENICpossibly homozygous992747462
1245482925245482926TG37GENICpossibly homozygous992747463
1245484706245484707AG24GENIChomozygous992747464
1245484741245484742AC32GENIChomozygous992747465
1245487389245487390TC25GENICpossibly homozygous992747466
1245487458245487459GA40GENICpossibly homozygous992747467
1245489679245489680GT15GENICpossibly homozygous992747468
1245500482245500483AG23GENICpossibly homozygous992747469
1245501182245501183TA30GENIChomozygous992747470
1245501635245501636AT34GENIChomozygous992747471
1245501692245501693CT28GENICpossibly homozygous992747472
1245503750245503751GA33GENICpossibly homozygous992747473
1245507013245507014TC32GENICpossibly homozygous992747474
1245508345245508346TC20GENICpossibly homozygous992747475
1245508617245508618GA14GENICpossibly homozygous992747476
1245509605245509606GA22GENICpossibly homozygous992747477
1245510582245510583CT30GENIChomozygous992747478
1245515748245515749AG21GENICpossibly homozygous992747479
1245516179245516180AG23GENICpossibly homozygous992747480