chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7118680557118680558AG58GENICheterozygous54079778
7118680684118680685GGTTGGGGAC35GENICheterozygous55000806
7118680860118680861TTCTTCTTC13GENICheterozygous55000808
7118681200118681201G-15GENIChomozygous54079785
7118681238118681239TC26GENIChomozygous54079786
7118681653118681654T-12GENIChomozygous54079788
7118681654118681655TC12GENIChomozygous55000810
7118681678118681679TC17GENIChomozygous54079789
7118681873118681874TC27GENIChomozygous54079790
7118681991118681994GGA---15GENIChomozygous54079792
7118682099118682100GA15GENIChomozygous54079793
7118682259118682260CG18GENIChomozygous54079794
7118683769118683773AGGC----13GENIChomozygous54079811
7118686386118686394AGATACAT--------25GENIChomozygous55000812
7118686435118686436TG26GENIChomozygous54079827
7118687070118687071CT40GENICheterozygous54079829
7118687335118687336AG44GENICheterozygous54079832
7118688004118688005G-36GENICheterozygous54920869
7118688012118688013GGA36GENICheterozygous54079836
7118688924118688925CT41GENICheterozygous54079841
7118689064118689065GC53GENICheterozygous54079842
7118689215118689216GA60GENICheterozygous54079844
7118689371118689372TTG47GENICheterozygous54079849
7118689749118689750TTA38GENICheterozygous54079862
7118689757118689758T-38GENICheterozygous54079863
7118690093118690094T-50GENICheterozygous54079872
7118691161118691162CG37GENICheterozygous54079882