chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1120858577120858578AC36GENIChomozygous992611089
1120861364120861365TG34GENICpossibly homozygous992611090
1120863522120863523GA18GENIChomozygous992611091
1120863587120863588TC23GENIChomozygous992611092
1120863618120863619CT27GENIChomozygous992611093
1120863621120863622TC30GENIChomozygous992611094
1120863785120863786CG27GENIChomozygous992611095
1120865644120865645AG6GENIChomozygous992611096
1120866083120866084TA23GENIChomozygous992611097