chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1107369519107369520TC18GENIChomozygous108909253
1107369886107369887CT22GENIChomozygous108909254
1107369908107369909GT24GENIChomozygous108168564
1107369919107369920AG23GENIChomozygous108168565
1107371149107371150TC19GENIChomozygous108168569
1107371613107371614CT27GENICpossibly homozygous108168570
1107371659107371660AG28GENIChomozygous108909255