chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X1506557115065572TC16GENIChomozygous953813732
X1506824715068248TC18GENIChomozygous953813733
X1506826015068261GA20GENIChomozygous953813734
X1507092415070925AG17GENIChomozygous953813735
X1507136615071367CT15GENIChomozygous953813736
X1507167115071672GA10GENIChomozygous953813737
X1507488115074882TA5GENIChomozygous953813738
X1507595315075954AC4GENIChomozygous953813739
X1508057915080580TG10GENIChomozygous953813740
X1508288115082882CA13GENIChomozygous953813741
X1508308515083086GA6GENIChomozygous953813742
X1508655315086554GC13GENIChomozygous953813743
X1508655615086557CG13GENIChomozygous953813744