chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X4496094244960943TA14GENIChomozygous108706687
X4496291244962913CT12GENIChomozygous108706689
X4496728044967281TC8GENIChomozygous108489575
X4496780744967808TC16GENIChomozygous108489577
X4496942244969423TC8GENICpossibly homozygous108489579
X4497169144971692AC15GENIChomozygous108706691
X4497482044974821CT15GENIChomozygous108489585
X4497768544977686CA24GENIChomozygous108706693
X4497936344979364AG12GENIChomozygous108489591
X4497973944979740CT17GENICpossibly homozygous108489593
X4498179644981797AC16GENIChomozygous108489597
X4498217844982179AG21GENIChomozygous108706695
X4498341644983417AT22GENIChomozygous108706697
X4498639444986395CA11GENIChomozygous108489601