chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
76486075664860757CG60GENIChomozygous115697760
76486075764860758CT60GENIChomozygous115697761
76486076064860761CT61GENIChomozygous115697762
76486076164860762CG62GENIChomozygous115697763
76486743864867438T70GENIChomozygous128473063
76486731264867312A50GENIChomozygous128473060
76486738664867387A53GENIChomozygous128473061
76486743164867432A67GENIChomozygous128473062
76486746664867466A73GENIChomozygous128473064
76486748064867480A75GENIChomozygous128473065
76486750164867503GA76GENIChomozygous128473066
76486750764867507C74GENIChomozygous128473067
76486755864867559A69GENIChomozygous128473068
76486758564867586CA61GENICpossibly homozygous115697770
76486765464867654A52GENIChomozygous128473069
76486767064867671A47GENIChomozygous128473070
76486768064867680A45GENIChomozygous128473071
76486777064867770G48GENIChomozygous128473072
76486777764867779TT48GENIChomozygous128473073
76486778264867783TA48GENIChomozygous118255038
76486761664867617AG56GENIChomozygous118255032
76486761764867618GT56GENIChomozygous118255034
76486778064867781TG48GENIChomozygous118255036
76486778264867782A47GENIChomozygous128473074
76486779364867793G48GENIChomozygous128473075
76486779664867798TG52GENIChomozygous128473076
76486780164867802TG52GENIChomozygous115697771
76486985864869858GAC51GENIChomozygous128473077
76487084764870848GT22GENIChomozygous115697772