chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
47090328970903290CT10GENIChomozygous112703686
47090381970903820GA10GENIChomozygous112703688
47090459570904596TA23GENIChomozygous112703690
47090465770904658GA28GENIChomozygous112703692
47090550270905503GT44GENIChomozygous112703694
47090750870907509GA22GENICpossibly homozygous112703696
47090861170908612AG26GENIChomozygous112703700
47090970570909706TC43GENIChomozygous112703702
47091041470910415CT43GENIChomozygous112703704
47091046370910464TC44GENIChomozygous112703706
47091089070910891CT28GENIChomozygous112703708
47091090970910910CT27GENIChomozygous112703710
47091265570912656AG36GENIChomozygous112703712
47091342470913425GA35GENIChomozygous112703714
47091603470916035TC26GENIChomozygous112703716
47091786270917863GA26GENIChomozygous112703718