chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X124635881124635882GC26GENIChomozygous992484650
X124636223124636224GA24GENIChomozygous992484651
X124642452124642453AG18GENIChomozygous992484652
X124643201124643202CT31GENIChomozygous992484653
X124644532124644533CT26GENIChomozygous992484654
X124644755124644756CT29GENIChomozygous992484655
X124648028124648029GT17GENIChomozygous992484656
X124648043124648044CT18GENIChomozygous992484657
X124648547124648548AG26GENIChomozygous992484658
X124648836124648837TC23GENIChomozygous992484659
X124651865124651866GC23GENIChomozygous992484660
X124651980124651981CT23GENIChomozygous992484661