chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X122940269122940270CG13GENIChomozygous108423639
X122941652122941653CT14GENIChomozygous108323573
X122942335122942336AG24GENIChomozygous108323575
X122943782122943783AG17GENIChomozygous108323577
X122944871122944872CA15GENIChomozygous108323579
X122944977122944978GA23GENIChomozygous108323581
X122945119122945120CG7GENIChomozygous108423641
X122945597122945598TC12GENIChomozygous108323583
X122945679122945680AG13GENIChomozygous108323585
X122947157122947158TA14GENIChomozygous108323587
X122947217122947218CG18GENIChomozygous108323589
X122947497122947498TG20GENIChomozygous108323593
X122948907122948908TC11GENIChomozygous108323597
X122950465122950466TA13GENIChomozygous108323601
X122950466122950467CA13GENIChomozygous108323603
X122950773122950774GA12GENIChomozygous108323605
X122952829122952830GA18GENIChomozygous108323607
X122953243122953244GC15GENIChomozygous108323609
X122953373122953374GA17GENIChomozygous108323611
X122953447122953448CT14GENIChomozygous108323613
X122953498122953499AT21GENIChomozygous108323615
X122954165122954166CT11GENIChomozygous108323617
X122956105122956106GA15GENIChomozygous108323619
X122956970122956971TC13GENIChomozygous108323621
X122958327122958328TG21GENIChomozygous108323623
X122959271122959272AG13GENIChomozygous108323625
X122959699122959700TC10GENIChomozygous108323629
X122959803122959804AG23GENIChomozygous108423645
X122962601122962602TC14GENIChomozygous108323633
X122963397122963398CA19GENIChomozygous108423647
X122967696122967697CA24GENIChomozygous108323637
X122968059122968060GA19GENIChomozygous108323639
X122969618122969619AG16GENIChomozygous108323643
X122970179122970180CT19GENIChomozygous108423650
X122971097122971098AG21GENIChomozygous108423652
X122971932122971933AC13GENIChomozygous108423654