chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7122150594122150595GC18GENIChomozygous54087457
7122150826122150827CCCA3GENICheterozygous54087458
7122153558122153559GA16GENIChomozygous54087463
7122154855122154856AATG1GENIChomozygous55144842
7122155180122155181AAG12GENIChomozygous54087465
7122155864122155865TC46GENIChomozygous54087466
7122156620122156621T-18GENICpossibly homozygous54511065
7122156951122156952AT19GENIChomozygous54087471
7122157951122157952CT16GENIChomozygous54087472
7122158468122158469CT16GENIChomozygous54087473
7122158658122158659TC21GENIChomozygous54087474
7122158661122158662AG19GENIChomozygous54087475
7122168155122168157TT--9GENICheterozygous54511137
7122168156122168157T-9GENICheterozygous55179802
7122173531122173543GTTTGTTTGTTT------------8GENIChomozygous54921295