chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104856968948569690A-5GENIChomozygous51640107
104857031448570315CCTTTCT2GENIChomozygous51640108
104857141348571414TC2GENIChomozygous51640109
104857142348571424GT5GENIChomozygous51640110
104857153448571535CCA14GENIChomozygous51447068
104857233548572336AG18GENIChomozygous51640111
104857303548573036GT22GENICpossibly homozygous51640112
104857352348573524TA25GENICpossibly homozygous51640113
104857366548573666GA23GENICheterozygous51640114
104857549748575498TC4GENICheterozygous51640116
104857788848577889CA15GENICpossibly homozygous51640118
104857823448578235TC7GENIChomozygous51640119
104857873048578734ACAC----2GENICheterozygous51640120
104857923748579238GGAA2GENIChomozygous51640122
104858219148582192GT20GENIChomozygous51640123
104858226548582266CT20GENIChomozygous51640124
104858284148582842GT8GENIChomozygous51640125
104858285548582856GA13GENIChomozygous51640126
104858288348582884GA27GENICpossibly homozygous51640127
104858294748582948CT23GENICpossibly homozygous51640128
104858296948582970AAC27GENIChomozygous51447078
104858522248585234TGTGTGTGTGTG------------1GENIChomozygous52561243