chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4130118890130118891AG21GENIChomozygous112827886
4130119584130119585GA18GENIChomozygous112827887
4130119703130119704AG20GENIChomozygous112827888
4130119788130119789AG12GENIChomozygous112827889
4130120299130120300GC19GENIChomozygous112827890
4130120327130120328GT20GENIChomozygous112827891
4130120412130120413AG11GENIChomozygous112827892
4130120498130120499CT17GENIChomozygous112827893
4130120670130120671AG19GENIChomozygous112827894
4130122753130122754CA20GENIChomozygous112827895
4130123651130123652CT10GENIChomozygous112827896
4130124853130124854GA21GENIChomozygous112827897
4130125288130125289CG15GENIChomozygous112827898
4130125675130125676TA19GENIChomozygous112827899
4130125945130125946GA14GENIChomozygous112827900
4130126387130126388CT14GENIChomozygous112827901
4130126895130126896AT22GENIChomozygous112827902
4130126914130126915AC26GENIChomozygous112827903
4130127929130127930TC15GENIChomozygous112827904
4130128109130128110AG13GENIChomozygous112827905
4130130168130130169GC13GENIChomozygous112827910
4130137678130137679GA25GENIChomozygous112827946
4130139679130139680GA16GENIChomozygous112827947
4130139870130139871TC12GENIChomozygous112827948
4130142623130142624TC20GENIChomozygous112827950
4130149501130149502TA16GENIChomozygous112827955
4130145916130145917AG17GENIChomozygous112827951
4130149739130149740AG14GENIChomozygous112827956
4130151578130151579AG26GENIChomozygous112827957
4130152109130152110TG13GENIChomozygous112827958