chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X1506557115065572TC7GENIChomozygous805546646
X1506630115066302GA20GENICheterozygous805546647
X1506824715068248TC10GENIChomozygous805546648
X1507092415070925AG10GENIChomozygous805546649
X1507167115071672GA19GENIChomozygous805546650
X1507700215077003GT27GENICheterozygous805546651
X1508288115082882CA10GENIChomozygous805546652
X1508655315086554GC20GENIChomozygous805546653
X1508655615086557CG19GENIChomozygous805546654