chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7130263548130263678AAAAATATTTAAGGGGTTGGGGATTTAGCTCAGTGGTAGAGCGCTTGCCTAGGAAGCGCAAGGCCCTGGGTTCGGTCCCCAGCTCTGGAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGAACCAAAAAAAA14GENIChomozygous128520266
7130263869130263870TC18GENIChomozygous115889669
7130264001130264030GGAGGACAGTCCTATGTGTATTGTGTGAG16GENIChomozygous128520267
7130264554130264555CT25GENIChomozygous115889677
7130265055130265056TC29GENIChomozygous115889679
7130265966130265981AAAACAAAGTTGACT19GENIChomozygous128520268
7130266609130266610TC33GENIChomozygous115889681
7130267073130267074AT26GENIChomozygous115889683
7130267182130267183GC27GENIChomozygous115889685
7130267217130267218CT24GENIChomozygous115889687
7130267486130267487AC29GENIChomozygous115889689
7130267498130267499TC25GENIChomozygous115889692
7130268656130268657CT21GENIChomozygous115889694
7130268681130268682TC19GENIChomozygous115889696
7130270754130270755TC37GENICpossibly homozygous115889698
7130271225130271229AGAT36GENIChomozygous128520269
7130271482130271482A33GENIChomozygous128520270
7130271916130271917TC28GENIChomozygous115889700
7130272607130272608TC39GENIChomozygous115889702
7130273416130273417GA38GENIChomozygous115889704
7130274101130274102AG33GENIChomozygous115889706
7130277368130277377AAGCAACAT28GENIChomozygous128520271
7130284801130284802CT31GENIChomozygous115889708
7130285606130285607AG30GENIChomozygous115889710
7130286818130286819CA29GENIChomozygous115889712
7130287675130287676CT37GENIChomozygous115889714