chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10109822388109822390TC--14INTERGENIChomozygous51600099
10109822740109822741GA29INTERGENIChomozygous51957707
10109823533109823541ACACACAC--------3INTERGENICheterozygous52734732
10109823818109823819AT22INTERGENIChomozygous51600120
10109824359109824360TC26INTERGENIChomozygous51600128
10109824420109824421AT34INTERGENIChomozygous51600130
10109824481109824482GA27INTERGENIChomozygous51957710
10109824533109824534GC24INTERGENIChomozygous51600132
10109824868109824869CT16INTERGENIChomozygous51600134
10109825331109825332G-18INTERGENICheterozygous52447963
10109825434109825435TC13INTERGENIChomozygous51600139
10109825909109825910CCAT15INTERGENIChomozygous51600142
10109826360109826364AAAA----10INTERGENIChomozygous51600147
10109826834109826835CT27INTERGENIChomozygous51957728
10109826933109826934GT23INTERGENIChomozygous51600154
10109827159109827160TC24INTERGENIChomozygous51600156
10109827273109827274TA18INTERGENIChomozygous51600157
10109826594109826595AAGG13INTERGENICheterozygous52410113
10109823804109823805AG11INTERGENIChomozygous52576047
10109823806109823807AT11INTERGENIChomozygous52576049
10109826594109826595AAGAGAGGGG13INTERGENICpossibly homozygous52576051
10109823814109823815CT16INTERGENIChomozygous52331863
10109825295109825298TTG---18INTERGENICheterozygous52331865