chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
47090328970903290CT15GENIChomozygous112703686
47090381970903820GA16GENIChomozygous112703688
47090459570904596TA35GENIChomozygous112703690
47090465770904658GA43GENICpossibly homozygous112703692
47090550270905503GT26GENIChomozygous112703694
47090750870907509GA20GENIChomozygous112703696
47090795370907954GC19GENIChomozygous112703698
47090861170908612AG21GENIChomozygous112703700
47090970570909706TC29GENIChomozygous112703702
47091041470910415CT36GENIChomozygous112703704
47091046370910464TC34GENIChomozygous112703706
47091089070910891CT27GENIChomozygous112703708
47091090970910910CT28GENIChomozygous112703710
47091265570912656AG29GENIChomozygous112703712
47091342470913425GA26GENIChomozygous112703714
47091603470916035TC24GENIChomozygous112703716
47091786270917863GA22GENIChomozygous112703718