chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
159017577390175774TC29GENIChomozygous112576637
159017578290175783AG30GENIChomozygous112576639
159017662090176621TA20GENIChomozygous112576641
159017670990176710TA11GENICpossibly homozygous112576643
159017725790177258TC26GENIChomozygous112576645