chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
173217408732174088AT34GENIChomozygous111028970
173217466032174661TC22GENIChomozygous111028972
173217476432174765AG16GENIChomozygous111028974
173217478332174784GT18GENIChomozygous111028976
173217505832175059AG25GENIChomozygous111028978
173217518532175186CT31GENIChomozygous111028980
173217562932175630CG24GENIChomozygous111028982
173217569132175692CT23GENIChomozygous111028984
173217572832175729AC22GENIChomozygous111028986
173217833032178331GA30GENIChomozygous111028988
173218093332180934GA27GENIChomozygous111028990
173218233832182339GA13GENIChomozygous119279278
173218741732187418GC35GENIChomozygous111481380
173218806132188062GC20GENICpossibly homozygous119279282