chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1176188507176188508TG28GENIChomozygous977978771
1176188574176188575CA29GENIChomozygous977978772
1176188845176188846CT52GENIChomozygous977978773
1176188972176188973GA50GENIChomozygous977978774
1176192382176192383TC10GENIChomozygous977978775
1176193196176193197AC14GENICpossibly homozygous977978776
1176193840176193841GA37GENIChomozygous977978777