chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4172121462172121463AG31GENIChomozygous112953409
4172122519172122520GA17GENIChomozygous113217537
4172124453172124454AG20GENIChomozygous112953419
4172128819172128820AG12GENIChomozygous112953423
4172129277172129278TC18GENIChomozygous113217559
4172125995172125999TCTT21GENIChomozygous128105070
4172129022172129024CC10GENIChomozygous130940635
4172129007172129008CT9GENIChomozygous113564119
4172129608172129609CT16GENIChomozygous113564121
4172124504172124505GC20GENIChomozygous113564117
4172124918172124919GA15GENIChomozygous113564118
4172129011172129012CT10GENIChomozygous113564120
4172130402172130403AG23GENIChomozygous113564122
4172130602172130603AG17GENIChomozygous112953425
4172132125172132126AG18GENIChomozygous112953429
4172132384172132385TC14GENIChomozygous112953431
4172132443172132444AG17GENIChomozygous112953433
4172132590172132591AG18GENIChomozygous112953435
4172132812172132813TG19GENIChomozygous112953437
4172132975172132976GA16GENIChomozygous113564123
4172133196172133206TGTCTCTGTG20GENIChomozygous130940637
4172133314172133315TC17GENIChomozygous112953439
4172133697172133698AG21GENIChomozygous112953445
4172133779172133780TG22GENIChomozygous112953447
4172133948172133949GA31GENIChomozygous113217563
4172133983172133984TC25GENIChomozygous112953449
4172134013172134014CT20GENIChomozygous113217564
4172133533172133534GA19GENIChomozygous113067984