chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4150316167150316168GA22GENIChomozygous57953034
4150316684150316685CA12GENIChomozygous57953037
4150316694150316695TC12GENIChomozygous56980684
4150316858150316859CG13GENIChomozygous56980685
4150317245150317246AT17GENIChomozygous56980686
4150317300150317301A-10GENIChomozygous58157026
4150317609150317627GTGTGTGTGTGTGTGTGT------------------5GENICheterozygous58346000
4150317611150317627GTGTGTGTGTGTGTGT----------------5GENICheterozygous58346002
4150317744150317745TA9GENIChomozygous56980687
4150317901150317902CT9GENIChomozygous58157028
4150318030150318031CT10GENICpossibly homozygous58157030
4150318787150318788TA8GENIChomozygous57953040
4150318823150318824TC10GENIChomozygous56980689
4150318909150318910GA12GENIChomozygous58157032
4150319228150319229TC7GENIChomozygous57953043