chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7130263548130263678AAAAATATTTAAGGGGTTGGGGATTTAGCTCAGTGGTAGAGCGCTTGCCTAGGAAGCGCAAGGCCCTGGGTTCGGTCCCCAGCTCTGGAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGAACCAAAAAAAA36GENIChomozygous128520266
7130263869130263870TC63GENIChomozygous115889669
7130264001130264030GGAGGACAGTCCTATGTGTATTGTGTGAG49GENIChomozygous128520267
7130264554130264555CT70GENIChomozygous115889677
7130267498130267499TC68GENIChomozygous115889692
7130265055130265056TC67GENIChomozygous115889679
7130266609130266610TC66GENIChomozygous115889681
7130267073130267074AT47GENIChomozygous115889683
7130267182130267183GC56GENIChomozygous115889685
7130267217130267218CT60GENIChomozygous115889687
7130265966130265981AAAACAAAGTTGACT60GENIChomozygous128520268
7130267486130267487AC66GENIChomozygous115889689
7130268656130268657CT64GENIChomozygous115889694
7130268681130268682TC61GENIChomozygous115889696
7130270754130270755TC65GENIChomozygous115889698
7130271225130271229AGAT65GENIChomozygous128520269
7130271482130271482A54GENIChomozygous128520270
7130271916130271917TC77GENIChomozygous115889700
7130272607130272608TC62GENIChomozygous115889702
7130273416130273417GA56GENIChomozygous115889704
7130274101130274102AG61GENIChomozygous115889706
7130277368130277377AAGCAACAT51GENIChomozygous128520271
7130284801130284802CT69GENIChomozygous115889708
7130285606130285607AG56GENIChomozygous115889710
7130286818130286819CA65GENICpossibly homozygous115889712
7130287675130287676CT75GENIChomozygous115889714