chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X122940269122940270CG8GENIChomozygous108423639
X122941652122941653CT11GENIChomozygous108323573
X122942335122942336AG16GENIChomozygous108323575
X122943782122943783AG5GENIChomozygous108323577
X122944871122944872CA10GENIChomozygous108323579
X122944977122944978GA11GENIChomozygous108323581
X122945119122945120CG14GENIChomozygous108423641
X122945597122945598TC16GENIChomozygous108323583
X122945679122945680AG12GENIChomozygous108323585
X122947157122947158TA7GENIChomozygous108323587
X122947217122947218CG6GENIChomozygous108323589
X122947497122947498TG15GENIChomozygous108323593
X122947719122947720AG7GENIChomozygous108323595
X122948907122948908TC12GENIChomozygous108323597
X122950465122950466TA13GENIChomozygous108323601
X122950466122950467CA12GENIChomozygous108323603
X122950773122950774GA13GENIChomozygous108323605
X122952829122952830GA11GENIChomozygous108323607
X122953243122953244GC11GENIChomozygous108323609
X122953373122953374GA13GENIChomozygous108323611
X122953447122953448CT15GENIChomozygous108323613
X122953498122953499AT16GENIChomozygous108323615
X122954165122954166CT14GENIChomozygous108323617
X122954849122954850GA3GENIChomozygous108423643
X122956105122956106GA13GENIChomozygous108323619
X122956970122956971TC16GENIChomozygous108323621
X122958327122958328TG13GENIChomozygous108323623
X122959271122959272AG8GENIChomozygous108323625
X122959699122959700TC9GENIChomozygous108323629
X122959803122959804AG9GENIChomozygous108423645
X122962601122962602TC8GENIChomozygous108323633
X122963397122963398CA11GENIChomozygous108423647
X122967696122967697CA9GENIChomozygous108323637
X122968059122968060GA9GENIChomozygous108323639
X122969618122969619AG20GENIChomozygous108323643
X122970179122970180CT10GENIChomozygous108423650
X122971097122971098AG9GENIChomozygous108423652
X122971932122971933AC6GENIChomozygous108423654
X122972990122972991CG14GENIChomozygous108423656