chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5105568885105568886GGA25GENIChomozygous56048674
5105569057105569058TC25GENIChomozygous55618881
5105569829105569830GGA18GENIChomozygous56048675
5105570089105570090TC16GENIChomozygous56048676
5105571248105571249AG33GENIChomozygous55618883
5105571985105571986TTA27GENIChomozygous56048677
5105574414105574415A-12GENICpossibly homozygous56048678
5105577938105577939CCG26GENIChomozygous55618887
5105582313105582324ATGCAAAAAAT-----------23GENIChomozygous56048679
5105586259105586260GA16GENIChomozygous56048680
5105586945105586949TCAG----19GENIChomozygous55618892
5105587020105587022AA--8GENICpossibly homozygous56048681
5105587021105587022A-8GENICheterozygous55618893
5105588219105588220GGT17GENIChomozygous55618895
5105588995105588997AA--3GENIChomozygous56048682
5105589114105589116AA--12GENICheterozygous55618898
5105589115105589116A-12GENICheterozygous55618899
5105591315105591316AT23GENIChomozygous56048683
5105595848105595849GC14GENICheterozygous55618901
5105597132105597133TA24GENICpossibly homozygous56048684
5105597845105597846AG15GENICheterozygous55618905
5105597849105597850CCAAA6GENIChomozygous55618906
5105599976105599978TC--16GENIChomozygous55618909