chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6117431926117431927AG28GENIChomozygous54665660
6117437025117437026TTTTA27GENIChomozygous54665662
6117437030117437031C-26GENIChomozygous54665664
6117437298117437299GGAA8GENICpossibly homozygous54665666
6117444995117444996AAG11GENICheterozygous54844826
6117444996117444998AG--11GENICpossibly homozygous54665668