chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X122940269122940270CG30GENIChomozygous108423639
X122941652122941653CT28GENIChomozygous108323573
X122942335122942336AG35GENIChomozygous108323575
X122943782122943783AG38GENIChomozygous108323577
X122944871122944872CA32GENIChomozygous108323579
X122944977122944978GA38GENIChomozygous108323581
X122945119122945120CG39GENIChomozygous108423641
X122945597122945598TC34GENIChomozygous108323583
X122945679122945680AG34GENIChomozygous108323585
X122947157122947158TA24GENIChomozygous108323587
X122947217122947218CG34GENIChomozygous108323589
X122947497122947498TG38GENIChomozygous108323593
X122947719122947720AG40GENIChomozygous108323595
X122948907122948908TC31GENIChomozygous108323597
X122950465122950466TA33GENIChomozygous108323601
X122950466122950467CA33GENIChomozygous108323603
X122950773122950774GA15GENIChomozygous108323605
X122952829122952830GA33GENIChomozygous108323607
X122953243122953244GC30GENIChomozygous108323609
X122953373122953374GA24GENIChomozygous108323611
X122953447122953448CT27GENIChomozygous108323613
X122953498122953499AT25GENIChomozygous108323615
X122954849122954850GA26GENIChomozygous108423643
X122956970122956971TC25GENIChomozygous108323621
X122954165122954166CT31GENIChomozygous108323617
X122956105122956106GA32GENIChomozygous108323619
X122958327122958328TG31GENIChomozygous108323623
X122959271122959272AG27GENIChomozygous108323625
X122959699122959700TC36GENIChomozygous108323629
X122959803122959804AG39GENIChomozygous108423645
X122962601122962602TC21GENIChomozygous108323633
X122963397122963398CA25GENIChomozygous108423647
X122967696122967697CA38GENIChomozygous108323637
X122968059122968060GA31GENIChomozygous108323639
X122969618122969619AG33GENIChomozygous108323643
X122970179122970180CT29GENIChomozygous108423650
X122971097122971098AG17GENIChomozygous108423652
X122971932122971933AC14GENIChomozygous108423654