chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2060752086075209CT14GENIChomozygous63574902
2060777086077709TA16GENIChomozygous63345358
2060777496077750TC19GENICheterozygous63574904
2060792486079249AT40GENICpossibly homozygous63345363
2060801836080184AG67GENICheterozygous63345364
2060814666081467AG54GENIChomozygous63345367
2060830626083063CG40GENICpossibly homozygous63574906
2060831886083189CT50GENIChomozygous63574908
2060846326084633GA43GENICpossibly homozygous63574910
2060854626085463CT65GENICpossibly homozygous63574912
2060881596088160TG41GENICheterozygous63574914
2060881626088163TG42GENICheterozygous63574916