chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7117766544117766545GA29GENIChomozygous115848093
7117767792117767793AG30GENIChomozygous115848095
7117769991117769992GA18GENICpossibly homozygous115848097
7117770415117770416CT12GENIChomozygous115848099
7117770808117770809CT34GENIChomozygous115848101
7117770929117770930CT39GENIChomozygous115848103
7117772229117772230GA35GENIChomozygous115848105
7117772995117772996GA23GENIChomozygous115848107
7117770227117770229AG20GENIChomozygous128510697
7117772201117772201GTGC24GENICpossibly homozygous128510698