chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
76486075664860757CG21GENIChomozygous115697760
76486075764860758CT21GENIChomozygous115697761
76486076064860761CT20GENIChomozygous115697762
76486076164860762CG20GENIChomozygous115697763
76486743864867438T14GENIChomozygous128473063
76486731264867312A10GENIChomozygous128473060
76486738664867387A12GENIChomozygous128473061
76486743164867432A13GENIChomozygous128473062
76486746664867466A20GENIChomozygous128473064
76486748064867480A22GENIChomozygous128473065
76486750164867503GA23GENIChomozygous128473066
76486750764867507C23GENIChomozygous128473067
76486755864867559A20GENIChomozygous128473068
76486758564867586CA23GENIChomozygous115697770
76486765464867654A15GENIChomozygous128473069
76486767064867671A15GENIChomozygous128473070
76486768064867680A15GENIChomozygous128473071
76486777064867770G15GENIChomozygous128473072
76486777764867779TT16GENIChomozygous128473073
76486778264867783TA15GENIChomozygous118255038
76486761664867617AG15GENIChomozygous118255032
76486761764867618GT15GENIChomozygous118255034
76486778064867781TG16GENIChomozygous118255036
76486778264867782A16GENIChomozygous128473074
76486779364867793G15GENIChomozygous128473075
76486779664867798TG15GENIChomozygous128473076
76486780164867802TG15GENIChomozygous115697771
76486985864869858GAC16GENIChomozygous128473077
76487084764870848GT10GENIChomozygous115697772
76487882664878827T14GENICheterozygous130561554