chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X3779366237793663TG10GENIChomozygous974391527
X3779369537793696TG14GENIChomozygous974391528
X3782448237824483TA8GENIChomozygous974391529
X3782448337824484AG8GENIChomozygous974391530
X3782451637824517TG9GENIChomozygous974391531
X3782451737824518CT9GENIChomozygous974391532
X3782473637824737GA4GENIChomozygous974391533
X3782473837824739AT4GENIChomozygous974391534
X3782497837824979TG3GENIChomozygous974391535
X3793746737937468CT6GENIChomozygous974391536
X3793772537937726CT12GENIChomozygous974391537
X3793772637937727TC12GENIChomozygous974391538
X3796746337967464TG4GENIChomozygous974391539
X3799591837995919GT3GENIChomozygous974391540
X3799833337998334GA3GENIChomozygous974391541
X3799833737998338GA3GENIChomozygous974391542
X3799833937998340GA3GENIChomozygous974391543
X3799834437998345GA4GENIChomozygous974391544
X3800476238004763TA10GENIChomozygous974391545
X3800508138005082GT8GENIChomozygous974391546
X3800522738005228TA4GENIChomozygous974391547
X3801385338013854GA6GENIChomozygous974391548
X3801395538013956AT5GENIChomozygous974391549
X3806253938062540AT7GENIChomozygous974391550
X3806265838062659CA9GENIChomozygous974391551
X3817042238170423TG20GENIChomozygous974391552