chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1242107574210758CA15GENICpossibly homozygous50002730
1242108514210852GGC4GENICheterozygous50002731
1242109234210924C-4GENICheterozygous50002732
1242113594211360C-13GENIChomozygous50002733
1242117194211720GA22GENICpossibly homozygous50002734
1242122924212293CT8GENIChomozygous50002735
1242123724212373TC7GENIChomozygous50002736
1242134184213419GA14GENICheterozygous50002738