chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X73754207375421TA14GENIChomozygous45082709
X73767047376705CG14GENIChomozygous45082710
X73774927377493GA8GENICpossibly homozygous45082711
X73798757379876A-4GENIChomozygous45251031
X73809417380942TTA6GENIChomozygous45082712
X73810327381033AT10GENIChomozygous45082713
X73848347384835TC14GENIChomozygous45082714
X73893697389370TTC6GENIChomozygous45082715
X73896187389619AG9GENICheterozygous45082716
X73920607392061GGT2GENIChomozygous45082719
X73955967395597AT8GENIChomozygous45082721
X73959737395974AT4GENIChomozygous45082722
X73968457396846AT6GENIChomozygous45082723
X73977457397750GTATG-----6GENIChomozygous45082724
X74034007403401T-1GENIChomozygous45082729
X74077097407710GA11GENIChomozygous45082737
X74078587407859T-12GENIChomozygous45082738
X74169427416943CT13GENICpossibly homozygous45082740
X74206807420681GT4GENIChomozygous45082741
X74206867420687GT2GENIChomozygous45082742
X74206907420691T-1GENIChomozygous45082743
X74256547425655C-20GENIChomozygous45082744
X74336657433666T-2GENICheterozygous45082746
X74377197437723GGAA----1GENIChomozygous45498385