chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
109028929390289294CT8GENIChomozygous68670084
109029156690291567TC26GENIChomozygous68670086
109029226390292264AG19GENIChomozygous68670088
109029325890293259AC10GENIChomozygous69195386
109029410890294109CG14GENIChomozygous68670090
109029481890294819CT25GENIChomozygous68670092
109029662290296623CT10GENICpossibly homozygous68165593
109029697990296980TC20GENIChomozygous68670094
109029753290297533CT27GENIChomozygous68670096
109030195190301952CT14GENIChomozygous68670098
109030261390302614TA27GENIChomozygous68670100
109030370690303707TC17GENIChomozygous68670102
109030484290304843AG28GENIChomozygous68670104
109029525190295252AG16GENICheterozygous68455326
109029526790295268GA17GENICheterozygous68455329