chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7123558713123558714AG22GENICpossibly homozygous54236683
7123558814123558815CT14GENICpossibly homozygous54236685
7123558817123558818CT14GENICpossibly homozygous54236687
7123558866123558867TC14GENICpossibly homozygous54236689
7123559007123559008AT8GENICheterozygous54236691
7123559473123559474TG27GENICpossibly homozygous54236693
7123559565123559566TG17GENIChomozygous54236695
7123559817123559818C-20GENIChomozygous54236697
7123559976123559977GT30GENIChomozygous54236699
7123560114123560115GA11GENIChomozygous54236701
7123560886123560887GT1GENIChomozygous54921474
7123561590123561591CT29GENICpossibly homozygous54236705
7123562446123562447TG24GENIChomozygous54236707
7123562616123562617GA26GENICpossibly homozygous54236709
7123562665123562666AG13GENIChomozygous54236711
7123562674123562675GC10GENIChomozygous54236713
7123562708123562709GC11GENICheterozygous54236715