chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
132592912525929126AG28GENIChomozygous800081898
132593149725931498AG47GENICpossibly homozygous800081899
132593329125933292TG21GENIChomozygous800081900
132593391625933917CT38GENIChomozygous800081901
132593396825933969AG39GENIChomozygous800081902
132594018025940181CA24GENICpossibly homozygous800081903
132594036925940370GA38GENICpossibly homozygous800081904
132594173625941737AG36GENIChomozygous800081905
132594751025947511GT27GENIChomozygous800081906