chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7130263869130263870TC22GENIChomozygous115889669
7130264010130264011TA22GENICpossibly homozygous115889671
7130264169130264170AG8GENIChomozygous115889675
7130264554130264555CT15GENIChomozygous115889677
7130265055130265056TC21GENIChomozygous115889679
7130266609130266610TC14GENICheterozygous115889681
7130267073130267074AT17GENIChomozygous115889683
7130267182130267183GC7GENIChomozygous115889685
7130267217130267218CT10GENIChomozygous115889687
7130267486130267487AC12GENIChomozygous115889689
7130267498130267499TC9GENIChomozygous115889692
7130268656130268657CT20GENIChomozygous115889694
7130268681130268682TC23GENIChomozygous115889696
7130270754130270755TC12GENIChomozygous115889698
7130271228130271229TC10GENIChomozygous126540152
7130271916130271917TC28GENIChomozygous115889700
7130272607130272608TC13GENIChomozygous115889702
7130273416130273417GA20GENIChomozygous115889704
7130274101130274102AG9GENIChomozygous115889706
7130280922130280923AG18GENIChomozygous126540153
7130280939130280940TG18GENIChomozygous126540154
7130284801130284802CT29GENIChomozygous115889708
7130285606130285607AG23GENIChomozygous115889710
7130286818130286819CA27GENIChomozygous115889712
7130287675130287676CT17GENIChomozygous115889714