chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X2237031322370314AG10GENIChomozygous974382738
X2237266122372662CT12GENIChomozygous974382739
X2237587022375871TG4GENIChomozygous974382740
X2237657522376576TC10GENICpossibly homozygous974382741
X2237846522378466CT12GENIChomozygous974382742
X2237881522378816CT14GENIChomozygous974382743
X2237961722379618TG6GENIChomozygous974382744
X2237982222379823TA11GENIChomozygous974382745
X2238001722380018CT8GENIChomozygous974382746
X2238011022380111AG12GENIChomozygous974382747
X2238015122380152GC4GENIChomozygous974382748
X2238087322380874TA3GENIChomozygous974382749
X2238141622381417CT13GENIChomozygous974382750
X2238148922381490CT12GENIChomozygous974382751
X2238229822382299AT5GENIChomozygous974382752
X2238265522382656TC6GENIChomozygous974382753
X2238347022383471AT6GENIChomozygous974382754
X2238435222384353GA6GENIChomozygous974382755
X2238436222384363AG4GENIChomozygous974382756
X2238472922384730TC6GENIChomozygous974382757
X2238521122385212AG12GENIChomozygous974382758
X2238557922385580AG9GENIChomozygous974382759
X2238798522387986CT5GENIChomozygous974382760
X2238829822388299TC6GENIChomozygous974382761
X2238838722388388TA6GENIChomozygous974382762
X2238917122389172CT5GENIChomozygous974382763
X2238927322389274GA9GENIChomozygous974382764
X2239033722390338AG9GENIChomozygous974382765
X2239565622395657TC10GENIChomozygous974382766