chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
183932074939320749T22GENICpossibly homozygous140219679
183932195439321955TA19GENIChomozygous140302764
183932208239322083TC20GENIChomozygous140302765
183932217639322177GT17GENIChomozygous140302766
183932421539324216AC32GENIChomozygous140302767
183932501939325020CT11GENIChomozygous140302768
183932545039325451GA18GENIChomozygous140302769
183932550539325506CG23GENIChomozygous140302770