chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8115345594115345595AG29INTERGENIChomozygous52825869
8115348404115348405A-16INTERGENICpossibly homozygous52825870
8115348891115348893TT--18INTERGENIChomozygous52825871
8115349013115349014A-18INTERGENIChomozygous52825874
8115349094115349095GA16INTERGENIChomozygous52825875
8115349246115349247AG23INTERGENIChomozygous52825876
8115349478115349479CT11INTERGENIChomozygous52825877
8115350909115350910CT16INTERGENIChomozygous52825878
8115351352115351368GTGTGTGTGCGCGTGC----------------6INTERGENIChomozygous52825879
8115351384115351385GA6INTERGENIChomozygous52825881
8115352899115352900GGA19INTERGENIChomozygous52825882
8115353018115353019TC16INTERGENIChomozygous52825883
8115354185115354186GGA19INTERGENIChomozygous52825884
8115354212115354218GAGGAG------19INTERGENIChomozygous52825885
8115354812115354813T-18INTERGENIChomozygous52825888
8115354813115354814GC18INTERGENIChomozygous53367951
8115356192115356193AATCG7INTERGENIChomozygous53579893
8115356753115356754CT25INTERGENIChomozygous52825893
8115357643115357644CT17INTERGENIChomozygous52825894
8115357890115357891TG15INTERGENIChomozygous52825895
8115357910115357911CT17INTERGENIChomozygous52825896