chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2061477716147772CT32GENICpossibly homozygous63345609
2061479176147918TC18GENIChomozygous63345613
2061480956148096TC14GENICpossibly homozygous63345614
2061490646149065GT24GENIChomozygous63574964
2061497356149736TC28GENIChomozygous63345616