chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X1506557115065572TC28GENIChomozygous980983769
X1506701415067015GA14GENIChomozygous980983770
X1506824715068248TC12GENICpossibly homozygous980983771
X1507092415070925AG23GENIChomozygous980983772
X1507338115073382GT8GENIChomozygous980983773
X1507342215073423CT7GENIChomozygous980983774
X1507348515073486CT12GENIChomozygous980983775
X1508074115080742CT26GENIChomozygous980983776
X1508288115082882CA22GENIChomozygous980983777
X1508377215083773AG13GENIChomozygous980983778