chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4145331182145331183GC17GENIChomozygous112870773
4145331516145331517CT18GENIChomozygous112870774
4145335610145335611GA23GENIChomozygous112870775
4145336099145336100AC12GENIChomozygous112870776
4145336235145336236GA18GENIChomozygous112870777
4145336818145336819CT18GENIChomozygous112870778
4145337170145337171CT11GENIChomozygous112870779
4145337437145337438AT15GENIChomozygous112870780
4145338534145338535GA13GENIChomozygous112870781
4145339352145339353TC19GENIChomozygous112870782
4145340736145340737CT30GENIChomozygous112870783
4145333715145333715G8GENIChomozygous128087955
4145335071145335072A14GENICpossibly homozygous128087956
4145335233145335237ATTT23GENIChomozygous128087957
4145339285145339285G14GENIChomozygous128087958