chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
171796724717967248GA22GENIChomozygous791593114
171796791517967916AG31GENIChomozygous791593115
171797336117973362AT21GENIChomozygous791593116
171797477917974780TC19GENIChomozygous791593117
171797659417976595TG30GENICpossibly homozygous791593118
171798065417980655TG17GENICpossibly homozygous791593119
171798257417982575AG13GENIChomozygous791593120
171798500017985001GA17GENIChomozygous791593121
171798569117985692AG17GENIChomozygous791593122
171798622417986225TC12GENIChomozygous791593123
171798775917987760GT20GENIChomozygous791593124