chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3151033541151033542AG16GENIChomozygous111776136
3151033664151033665GA18GENIChomozygous112041292
3151033748151033749GT14GENIChomozygous112041294
3151033863151033864GA16GENIChomozygous111776138
3151034572151034573GA12GENIChomozygous111776139
3151035246151035247TC15GENIChomozygous112041296
3151037586151037587AG18GENIChomozygous111776141
3151037672151037673GA21GENIChomozygous112041300
3151037969151037970CT24GENIChomozygous112041302
3151038882151038883TC13GENIChomozygous111776145
3151039340151039341GA18GENIChomozygous112041304
3151039734151039735CT11GENIChomozygous112041306
3151042440151042441GA8GENIChomozygous111776147
3151047008151047009AG27GENIChomozygous111776151
3151047626151047627GA13GENIChomozygous112041310
3151047712151047713TC19GENIChomozygous112041312
3151048099151048100GA21GENIChomozygous112041314
3151048588151048589AC13GENIChomozygous112041316
3151050323151050324GA21GENIChomozygous112041318
3151050389151050390CT22GENIChomozygous112041320
3151050488151050489CT12GENIChomozygous112041322
3151051368151051369TC25GENIChomozygous112041324
3151051649151051650TC14GENIChomozygous112041326
3151052105151052106TC24GENIChomozygous112041328
3151054940151054941AG21GENIChomozygous112041330
3151057450151057451TC26GENIChomozygous112041332
3151060499151060500GA9GENIChomozygous112041336
3151064699151064700GA14GENIChomozygous112041340
3151065901151065902GA24GENIChomozygous112041342
3151071778151071779GC19GENIChomozygous112041344
3151073688151073689CT20GENIChomozygous111776165
3151074452151074453GT23GENICpossibly homozygous112041352
3151040417151040418CA7GENICheterozygous119939401
3151041221151041222GA11GENIChomozygous119652284