chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X73754207375421TA8GENIChomozygous45082709
X73767047376705CG31GENIChomozygous45082710
X73774927377493GA12GENIChomozygous45082711
X73809417380942TTA9GENIChomozygous45082712
X73810327381033AT10GENIChomozygous45082713
X73848347384835TC20GENIChomozygous45082714
X73893697389370TTC8GENIChomozygous45082715
X73896187389619AG16GENIChomozygous45082716
X73915647391565AAT4GENICheterozygous45082717
X73915677391568AAT2GENIChomozygous45082718
X73920607392061GGT2GENICheterozygous45082719
X73949047394907AAA---2GENIChomozygous45082720
X73955967395597AT21GENIChomozygous45082721
X73959737395974AT7GENIChomozygous45082722
X73968457396846AT10GENIChomozygous45082723
X73977457397750GTATG-----5GENIChomozygous45082724
X73980487398050AA--9GENIChomozygous45082725
X74015677401568GT11GENICheterozygous45082726
X74015877401588G-11GENICpossibly homozygous45082727
X74015897401592TAG---11GENICheterozygous45082728
X74034007403401T-12GENICpossibly homozygous45082729
X74038967403897A-10GENIChomozygous45082730
X74040247404025TC16GENICpossibly homozygous45082731
X74054087405430ATATATATATATATATATATAT----------------------2GENIChomozygous45082732
X74055527405553GA19GENICheterozygous45082733
X74055567405557AC19GENICheterozygous45082734
X74055607405561CT22GENICheterozygous45082735
X74055687405569AG24GENICheterozygous45082736
X74077097407710GA7GENIChomozygous45082737
X74078587407859T-5GENIChomozygous45082738
X74146397414640AAG3GENIChomozygous45082739
X74169427416943CT9GENIChomozygous45082740
X74206807420681GT11GENIChomozygous45082741
X74206867420687GT12GENIChomozygous45082742
X74206907420691T-12GENIChomozygous45082743
X74256547425655C-8GENIChomozygous45082744
X74274387427439CCT6GENICheterozygous45082745
X74336657433666T-14GENIChomozygous45082746
X74377577437758AG4GENIChomozygous45082747