chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1670862517086252TA49GENICpossibly homozygous112219823
1670884277088428CT52GENIChomozygous111712293
1670892457089246GC38GENIChomozygous111712295
1670904037090404GA39GENIChomozygous111712297
1670906797090680CA35GENIChomozygous111712299
1670926247092625AC28GENICpossibly homozygous111712301
1670940647094065GA36GENIChomozygous111712303
1670941327094133AG38GENIChomozygous111712305
1670944397094440CT22GENIChomozygous112219824
1670945507094551GA12GENIChomozygous112221658
1670945647094565CT10GENIChomozygous112274614
1670945687094569CT7GENIChomozygous112274617
1670945717094572GA7GENIChomozygous112274619
1670945747094575CT7GENIChomozygous112274622
1670964287096429GA49GENIChomozygous111712307