chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10109822388109822390TC--12INTERGENIChomozygous51600099
10109823509109823510TA14INTERGENIChomozygous51600107
10109823539109823541AC--2INTERGENIChomozygous52410111
10109823804109823807ATA---2INTERGENIChomozygous51600116
10109823814109823815CT7INTERGENIChomozygous52331863
10109823818109823819AT8INTERGENIChomozygous51600120
10109824359109824360TC13INTERGENIChomozygous51600128
10109824420109824421AT15INTERGENICpossibly homozygous51600130
10109824481109824482GA19INTERGENIChomozygous51957710
10109824533109824534GC20INTERGENIChomozygous51600132
10109824868109824869CT17INTERGENIChomozygous51600134
10109825434109825435TC12INTERGENIChomozygous51600139
10109825909109825910CCAT11INTERGENIChomozygous51600142
10109826361109826364AAA---2INTERGENICheterozygous51600148
10109826594109826595AAGG7INTERGENIChomozygous52410113
10109826834109826835CT16INTERGENIChomozygous51957728
10109826933109826934GT22INTERGENIChomozygous51600154
10109827159109827160TC32INTERGENIChomozygous51600156
10109827273109827274TA17INTERGENIChomozygous51600157
10109825331109825332G-30INTERGENICheterozygous52447963