chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7141293368141293369TC22GENICpossibly homozygous115939885
7141293544141293545AG28GENICpossibly homozygous115939886
7141294751141294752TA25GENIChomozygous115939887
7141294849141294850CT20GENIChomozygous115939888
7141297421141297422CA18GENIChomozygous115939889
7141297431141297432TG18GENIChomozygous115939890
7141299203141299204GA33GENIChomozygous115939891
7141303428141303429CT21GENIChomozygous115939892
7141304205141304206AG22GENIChomozygous115939893