chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7118680557118680558AG70GENICheterozygous54079778
7118680684118680685GGTTGGGGAC37GENICheterozygous55000806
7118681200118681201G-26GENIChomozygous54079785
7118681238118681239TC33GENIChomozygous54079786
7118681653118681654T-14GENIChomozygous54079788
7118681654118681655TC14GENIChomozygous55000810
7118681678118681679TC20GENIChomozygous54079789
7118681873118681874TC32GENIChomozygous54079790
7118681991118681994GGA---36GENIChomozygous54079792
7118682099118682100GA18GENIChomozygous54079793
7118682259118682260CG8GENIChomozygous54079794
7118683769118683773AGGC----14GENIChomozygous54079811
7118686386118686394AGATACAT--------13GENICpossibly homozygous55000812
7118686435118686436TG15GENIChomozygous54079827
7118687070118687071CT34GENICheterozygous54079829
7118687335118687336AG49GENICheterozygous54079832
7118688012118688013GGA54GENICheterozygous54079836
7118688924118688925CT57GENICheterozygous54079841
7118689064118689065GC49GENICheterozygous54079842
7118689215118689216GA49GENICheterozygous54079844
7118689371118689372TTG32GENICheterozygous54079849
7118689749118689750TTA37GENICheterozygous54079862
7118689757118689758T-36GENICheterozygous54079863
7118690093118690094T-31GENICheterozygous54079872
7118691161118691162CG35GENICheterozygous54079882
7118688004118688005G-54GENICheterozygous54920869