chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5144581359144581360GT22GENICpossibly homozygous114037451
5144582641144582642CA11GENIChomozygous114037452
5144598389144598390GA17GENIChomozygous114037453
5144600435144600436GA28GENIChomozygous114037454
5144600974144600975CT32GENIChomozygous114037455
5144604576144604577CG14GENICheterozygous114037457
5144604580144604581CG15GENICheterozygous114037458
5144604584144604585CG15GENICheterozygous114037459
5144605215144605216TC16GENIChomozygous114037460
5144607899144607900CT12GENIChomozygous114037461
5144609035144609036GA19GENIChomozygous114037462
5144611073144611074TC14GENIChomozygous114037463
5144604592144604593CG14GENICheterozygous114152422
5144604588144604589CG14GENICheterozygous114152421