chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X73754207375421TA13GENIChomozygous657067707
X73767047376705CG11GENIChomozygous657067708
X73774927377493GA8GENIChomozygous657067709
X73798757379876A-6GENIChomozygous761270208
X73806577380658TTAC1GENIChomozygous761270210
X73809417380942TTA7GENIChomozygous761270211
X73810327381033AT12GENIChomozygous657067710
X73848347384835TC15GENIChomozygous657067711
X73893697389370TTC10GENIChomozygous761270212
X73896187389619AG18GENIChomozygous657067712
X73915647391565AAT4GENIChomozygous761270213
X73920607392061GGT8GENICpossibly homozygous761270214
X73955967395597AT12GENIChomozygous657067713
X73959737395974AT13GENIChomozygous657067714
X73968457396846AT11GENIChomozygous657067715
X73977457397750GTATG-----15GENIChomozygous761270215
X73980487398050AA--7GENIChomozygous761270216
X74015877401588G-6GENIChomozygous761270217
X74015897401592TAG---6GENIChomozygous761270218
X74034007403401T-8GENIChomozygous761270219
X74038967403897A-15GENICpossibly homozygous761270220
X74040247404025TC8GENICpossibly homozygous657067716
X74054087405430ATATATATATATATATATATAT----------------------10GENIChomozygous761270221
X74077097407710GA13GENIChomozygous657067717
X74078587407859T-7GENIChomozygous761270222
X74134877413513TGTGTGTGTGTGTGTGTGTGTGTGTG--------------------------8GENIChomozygous761270224
X74146397414640AAG4GENIChomozygous761270225
X74169427416943CT6GENIChomozygous657067718
X74186637418665GC--5GENICheterozygous761270226
X74206807420681GT17GENIChomozygous657067719
X74206867420687GT18GENIChomozygous657067720
X74206907420691T-17GENIChomozygous761270227
X74256547425655C-9GENIChomozygous761270228
X74274387427439CCT6GENICheterozygous761270229
X74321127432120CACACACA--------3GENIChomozygous761270230
X74329217432927TGTGTG------2GENIChomozygous761270231
X74336657433666T-7GENIChomozygous761270233
X74367257436726A-6GENIChomozygous761270234
X74377197437723GGAA----2GENIChomozygous761270235