chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
41031606610316067AG26GENIChomozygous56745823
41031662110316622AT8GENICpossibly homozygous56745824
41031818510318186GT29GENICpossibly homozygous56745826
41031908010319081CT24GENIChomozygous56745827
41031909610319097T-19GENIChomozygous56745828
41031959310319594CT18GENICpossibly homozygous56745829
41032021410320215GGAC7GENICpossibly homozygous58274348