chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X135305276135305277GA16GENIChomozygous125170786
X135307508135307509T3GENIChomozygous132781881
X135310414135310415CT11GENICpossibly homozygous125170787
X135310756135310756ACTT7GENIChomozygous132781883
X135310909135310910GT7GENICpossibly homozygous125170788
X135311150135311151CA12GENIChomozygous125170789
X135317507135317508AG10GENIChomozygous125170790
X135318858135318859GA16GENIChomozygous125170791
X135326351135326352A8GENIChomozygous132781886
X135309928135309929GA9GENIChomozygous135388666
X135327512135327513CT6GENIChomozygous108510066
X135330610135330611TC11GENIChomozygous108510070
X135331276135331277A13GENIChomozygous132781888
X135335870135335871TC5GENIChomozygous108510082
X135337617135337618GT15GENIChomozygous108510086
X135339089135339090AG8GENIChomozygous108510088
X135342489135342490GT12GENIChomozygous108510098
X135337133135337133A12GENIChomozygous129793741
X135338487135338488TC4GENIChomozygous108821374