chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
66972127569721276CT27GENICpossibly homozygous54895984
66972272869722729AG18GENIChomozygous54487138
66972386669723867GGA1GENIChomozygous54487144
66972457669724577GC11GENICpossibly homozygous54487148
66972490569724906CT5GENIChomozygous54487154
66972537269725373TTAAAAA1GENIChomozygous55650572
66972662369726624AACAGTCAC8GENIChomozygous54487167
66972790069727901CT8GENICpossibly homozygous54487185
66972823669728237CCT10GENIChomozygous54487189
66972998569729986C-2GENIChomozygous54895988
66973006169730062A-16GENIChomozygous54895990
66973060869730609CA14GENIChomozygous54895992
66973151869731520AG--9GENIChomozygous54487207
66973220469732205GT19GENIChomozygous54895994
66973311769733118CCTTA10GENIChomozygous54487209
66973324169733242GA15GENICpossibly homozygous54895995
66973440869734409TG18GENIChomozygous54895999
66973634669736347A-2GENIChomozygous54896001
66973772069737721TTG13GENICheterozygous54487223
66973894069738941AG3GENICheterozygous54487225