chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
122224593622245937GA39GENIChomozygous781775113
122224594122245942CT42GENICheterozygous781775114
122224693322246934GA50GENIChomozygous781775115
122224698322246984CA49GENIChomozygous781775116
122224726922247270AG44GENIChomozygous781775117
122224750222247503CG58GENIChomozygous781775118
122224879522248796AG41GENICpossibly homozygous781775119
122225148622251487TC33GENIChomozygous781775120