chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7118007751118007752TC36GENIChomozygous54078944
7118008506118008507GGT28GENICpossibly homozygous54078945
7118008617118008618AC43GENIChomozygous54078946
7118008673118008674AAT13GENICheterozygous54078947
7118008674118008675T-13GENICheterozygous54078948
7118008688118008689TA28GENICpossibly homozygous54078949
7118008915118008916GGT13GENIChomozygous54078950
7118008964118008965GA21GENIChomozygous54078951
7118009695118009696CG46GENIChomozygous54078952