chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X73754207375421TA14GENIChomozygous45082709
X73767047376705CG9GENIChomozygous45082710
X73774927377493GA14GENIChomozygous45082711
X73798757379876A-12GENIChomozygous45251031
X73806577380658TTAC3GENIChomozygous45498373
X73809417380942TTA9GENIChomozygous45082712
X73810327381033AT18GENIChomozygous45082713
X73848347384835TC15GENIChomozygous45082714
X73893697389370TTC12GENIChomozygous45082715
X73896187389619AG12GENIChomozygous45082716
X73915647391565AAT8GENIChomozygous45082717
X73920607392061GGT3GENIChomozygous45082719
X73953737395374TTTGTG8GENIChomozygous45498375
X73955967395597AT7GENIChomozygous45082721
X73959737395974AT18GENIChomozygous45082722
X73968457396846AT11GENIChomozygous45082723
X73977457397750GTATG-----15GENIChomozygous45082724
X73980487398050AA--4GENIChomozygous45082725
X74015877401588G-2GENIChomozygous45082727
X74015897401592TAG---2GENIChomozygous45082728
X74034007403401T-5GENICheterozygous45082729
X74038967403897A-7GENIChomozygous45082730
X74040247404025TC10GENIChomozygous45082731
X74054087405430ATATATATATATATATATATAT----------------------9GENIChomozygous45082732
X74077097407710GA10GENIChomozygous45082737
X74078587407859T-16GENIChomozygous45082738
X74134877413513TGTGTGTGTGTGTGTGTGTGTGTGTG--------------------------5GENIChomozygous45498379
X74146397414640AAG3GENICheterozygous45082739
X74169427416943CT11GENIChomozygous45082740
X74206807420681GT6GENIChomozygous45082741
X74206867420687GT6GENIChomozygous45082742
X74206907420691T-6GENIChomozygous45082743
X74256547425655C-10GENIChomozygous45082744
X74274387427439CCT9GENIChomozygous45082745
X74321127432120CACACACA--------1GENIChomozygous45498383
X74329217432927TGTGTG------7GENIChomozygous45662435
X74336657433666T-7GENIChomozygous45082746
X74367257436726A-5GENIChomozygous45251035
X74214667421476CACACACACA----------1GENIChomozygous45783330
X74184857418486AATTTC2GENIChomozygous45564690