chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X122940269122940270CG5GENIChomozygous108423639
X122941652122941653CT8GENIChomozygous108323573
X122942335122942336AG11GENIChomozygous108323575
X122943782122943783AG9GENIChomozygous108323577
X122944871122944872CA13GENIChomozygous108323579
X122944977122944978GA16GENIChomozygous108323581
X122945119122945120CG15GENIChomozygous108423641
X122945597122945598TC14GENIChomozygous108323583
X122945679122945680AG11GENIChomozygous108323585
X122947157122947158TA15GENIChomozygous108323587
X122947217122947218CG18GENIChomozygous108323589
X122947497122947498TG19GENIChomozygous108323593
X122947719122947720AG10GENIChomozygous108323595
X122948907122948908TC13GENIChomozygous108323597
X122950465122950466TA15GENIChomozygous108323601
X122950466122950467CA15GENIChomozygous108323603
X122950773122950774GA14GENIChomozygous108323605
X122952829122952830GA18GENIChomozygous108323607
X122953243122953244GC18GENIChomozygous108323609
X122953373122953374GA14GENIChomozygous108323611
X122953447122953448CT21GENIChomozygous108323613
X122953498122953499AT27GENIChomozygous108323615
X122954165122954166CT15GENIChomozygous108323617
X122956105122956106GA18GENIChomozygous108323619
X122956970122956971TC20GENIChomozygous108323621
X122958327122958328TG18GENIChomozygous108323623
X122959271122959272AG16GENIChomozygous108323625
X122959699122959700TC9GENIChomozygous108323629
X122959803122959804AG14GENIChomozygous108423645
X122962601122962602TC19GENIChomozygous108323633
X122963397122963398CA13GENIChomozygous108423647
X122967696122967697CA14GENIChomozygous108323637
X122968059122968060GA11GENIChomozygous108323639
X122969618122969619AG12GENIChomozygous108323643
X122970179122970180CT18GENIChomozygous108423650
X122971097122971098AG11GENIChomozygous108423652
X122971932122971933AC9GENIChomozygous108423654
X122972990122972991CG14GENIChomozygous108423656