chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
47090437970904380GA18GENIChomozygous119433816
47090550270905503GT21GENIChomozygous112703694
47090861170908612AG24GENIChomozygous112703700
47090970570909706TC32GENIChomozygous112703702
47090993370909934AG27GENIChomozygous119433817
47091046370910464TC34GENIChomozygous112703706
47091089070910891CT15GENIChomozygous112703708
47091195870911959GA36GENIChomozygous119433818
47091212770912128CT29GENIChomozygous113032994
47091322470913225CG32GENICpossibly homozygous119433819
47091342470913425GA25GENIChomozygous112703714
47091786270917863GA24GENIChomozygous112703718