chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
41031606610316067AG18GENIChomozygous56745823
41031662110316622AT9GENIChomozygous56745824
41031670610316707GGT11GENICpossibly homozygous56745825
41031818510318186GT12GENIChomozygous56745826
41031908010319081CT24GENIChomozygous56745827
41031909610319097T-20GENIChomozygous56745828
41031959310319594CT22GENIChomozygous56745829
41032015010320151TTACAC4GENICheterozygous58327036
41032021410320215GGAC20GENICpossibly homozygous58274348