chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3138026275138026276GA17GENIChomozygous112307490
3138026753138026754GT15GENIChomozygous111743374
3138028015138028016AG14GENIChomozygous111743378
3138028379138028380CT8GENIChomozygous125838648
3138029321138029322AG15GENIChomozygous111743380
3138029402138029403GA11GENIChomozygous111743382
3138029721138029722AG19GENIChomozygous111743386
3138029873138029874TC17GENIChomozygous111743388
3138036146138036147GA19GENIChomozygous112307493
3138037409138037410AT8GENIChomozygous125838649
3138038184138038185GA23GENIChomozygous112307495
3138039388138039389CT22GENIChomozygous112307497
3138040539138040540AG17GENIChomozygous111743400
3138040959138040960TC15GENIChomozygous111743402
3138041793138041794GA16GENIChomozygous111743404
3138042670138042671GA7GENIChomozygous112307499
3138042784138042785GA7GENIChomozygous125867947
3138048281138048282TC28GENICpossibly homozygous112307505