chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1213765979213765980TG12GENIChomozygous108531856
1213766176213766177AG23GENIChomozygous108531857
1213766894213766895CA26GENIChomozygous108531860
1213767110213767111GT24GENIChomozygous109191625
1213767162213767163AG19GENICpossibly homozygous108531861
1213767604213767605TC24GENIChomozygous108531862