chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7142770008142770015GCTACTT26GENIChomozygous131025889
7142770422142770423GT24GENIChomozygous116098628
7142771672142771673GT17GENIChomozygous116098630
7142772200142772201AG30GENIChomozygous116098632
7142772740142772741AG22GENIChomozygous116098634
7142773617142773618AG27GENIChomozygous116098636
7142773730142773731TC21GENIChomozygous116098638
7142774012142774013CT26GENIChomozygous116098640
7142775750142775751GA19GENIChomozygous116098642
7142776123142776123T19GENICpossibly homozygous131025890
7142779253142779253CT25GENIChomozygous128530810
7142783266142783271GGGCT8GENIChomozygous128530811