chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141852378618523787CA3GENIChomozygous131148973
141852463518524636TA5GENIChomozygous113810343
141852585318525854AG14GENIChomozygous113366536
141852840818528409AG14GENIChomozygous113366538
141852938918529390A14GENIChomozygous129130956
141852939018529391AG14GENIChomozygous113366540
141852954018529541GA22GENIChomozygous113366547
141852966118529665GCCT21GENICpossibly homozygous129130957
141852972418529725A21GENIChomozygous129130958
141852999918530000GA18GENIChomozygous113366549
141853070818530709AG25GENIChomozygous113366551
141852453518524536GC13GENIChomozygous113664097
141852525418525255GC10GENIChomozygous113664099
141852582718525828GA14GENIChomozygous113664101
141853028718530288GA20GENIChomozygous113664105
141852464018524640GTGGGGTAAGG2GENIChomozygous132897701
141852912818529128A16GENIChomozygous131142297