chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7141503097141503098G-23GENIChomozygous54159157
7141504099141504100AT10GENIChomozygous54159158
7141504453141504454G-3GENIChomozygous54159159
7141505684141505685GC18GENIChomozygous54159161
7141505712141505713TC26GENIChomozygous54159162
7141507035141507036AG13GENICpossibly homozygous54159163
7141507517141507518GT9GENIChomozygous54159164
7141507520141507521GA10GENIChomozygous54159165
7141507805141507806CG12GENICpossibly homozygous54159166
7141508892141508893GA12GENICheterozygous54159168
7141510823141510824C-7GENIChomozygous54159171
7141513148141513149CCTA14GENIChomozygous54159172
7141513308141513309TC16GENIChomozygous54159173
7141514955141514956AG18GENICpossibly homozygous54159174
7141515309141515310GC21GENICpossibly homozygous54159175
7141515698141515699AG20GENICpossibly homozygous54159176
7141515839141515840GC12GENICpossibly homozygous54159177
7141516306141516307TTA17GENIChomozygous54159182