chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X3779361237793613AG24GENIChomozygous778240771
X3779366237793663TG22GENIChomozygous778240772
X3779369537793696TG13GENIChomozygous778240773
X3782468737824688CG9GENIChomozygous778240774
X3782497837824979TG13GENIChomozygous778240775
X3785443737854438GA16GENICheterozygous778240776
X3787046937870470CA35GENICheterozygous778240777
X3791448137914482CA10GENIChomozygous778240778
X3791450337914504CG7GENIChomozygous778240779
X3791914237919143CT9GENICpossibly homozygous778240780
X3792409537924096GC250GENICheterozygous778240781
X3792442437924425GT84GENICheterozygous778240782
X3792442537924426GA85GENICheterozygous778240783
X3792444137924442CT95GENICheterozygous778240784
X3792448037924481GA91GENICheterozygous778240785
X3792451037924511GT82GENICheterozygous778240786
X3792451637924517AG86GENICheterozygous778240787
X3792453937924540CT74GENICheterozygous778240788
X3792457037924571GT60GENICheterozygous778240789
X3793179637931797GT27GENIChomozygous778240790
X3793721437937215CA6GENIChomozygous778240791
X3793799837937999AC9GENIChomozygous778240792
X3796746337967464TG11GENICpossibly homozygous778240793
X3799833337998334GA9GENIChomozygous778240794
X3799833737998338GA10GENIChomozygous778240795
X3799833937998340GA10GENIChomozygous778240796
X3799834437998345GA10GENIChomozygous778240797
X3800465938004660TA21GENIChomozygous778240798
X3800478538004786TG19GENIChomozygous778240799
X3800485238004853GC9GENIChomozygous778240800
X3800516338005164GA9GENIChomozygous778240801
X3801395538013956AT9GENIChomozygous778240802
X3806253938062540AT7GENICheterozygous778240803
X3806263038062631AT7GENIChomozygous778240804
X3806265838062659CA7GENIChomozygous778240805
X3806274638062747GT22GENICpossibly homozygous778240806
X3814242938142430GA25GENICheterozygous778240807
X3815618538156186AG98GENICheterozygous778240808
X3817042238170423TG26GENIChomozygous778240809