chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1242107574210758CA52GENIChomozygous50002730
1242108514210852GGC17GENICpossibly homozygous50002731
1242109234210924C-28GENIChomozygous50002732
1242113594211360C-44GENIChomozygous50002733
1242117194211720GA58GENIChomozygous50002734
1242122924212293CT51GENICpossibly homozygous50002735
1242123724212373TC58GENIChomozygous50002736
1242130594213060CT50GENIChomozygous50002737
1242134184213419GA66GENIChomozygous50002738