chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3151512638151512639CT21GENIChomozygous112310751
3151517534151517535AG25GENIChomozygous111777672
3151519994151519995GC18GENIChomozygous111777676
3151522448151522449CA10GENIChomozygous112310753
3151523454151523455AG12GENIChomozygous111777684
3151524143151524144GT11GENIChomozygous112310755
3151526739151526740TC27GENIChomozygous111777688
3151528785151528786AG13GENIChomozygous111777692
3151530256151530257CT16GENICpossibly homozygous111777694
3151531761151531762TC9GENIChomozygous111777696
3151535190151535191AG3GENIChomozygous111777698
3151535237151535238CT8GENIChomozygous112310757
3151539359151539360AG14GENIChomozygous112310759
3151540068151540069CT16GENIChomozygous112310761
3151541015151541016AG11GENIChomozygous111777700
3151542729151542730CT16GENIChomozygous112310763
3151543171151543172AG12GENIChomozygous111777702