chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1213765979213765980TG45GENICpossibly homozygous108531856
1213766176213766177AG51GENIChomozygous108531857
1213766534213766535GT41GENICpossibly homozygous108531858
1213766894213766895CA42GENIChomozygous108531860
1213767162213767163AG44GENIChomozygous108531861
1213767604213767605TC36GENIChomozygous108531862