chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
136780804367808044GA21GENIChomozygous66325643
136780884767808848GA17GENIChomozygous66325647
136780920567809206GT10GENIChomozygous66325649
136780962067809621TC21GENIChomozygous66076610
136780985967809860CA14GENIChomozygous66325651
136780991067809911AG14GENIChomozygous66076613
136781274967812750AT18GENIChomozygous66325653
136781343367813434TC25GENIChomozygous66325657
136781358667813587TC26GENIChomozygous66076627
136781479367814794AG13GENIChomozygous66325659
136781517567815176CT9GENIChomozygous66325661
136781668867816689GC5GENIChomozygous66633947
136781876167818762CG10GENIChomozygous66076633
136781975667819757GA16GENIChomozygous66325665
136782061967820620TC25GENIChomozygous66325667
136782257667822577TC6GENIChomozygous66076636
136782273767822738TC13GENIChomozygous66076639
136782299567822996AG14GENIChomozygous66076641
136782304667823047AC13GENIChomozygous66076644
136782304767823048GT13GENIChomozygous66076647
136782439567824395G16GENICheterozygous67026174
136781539567815396A22GENICheterozygous66868085
136781228567812285ATT5GENIChomozygous67026170
136781738667817386T26GENICheterozygous67026172
136782604967826050GA19GENIChomozygous66076656
136782650767826508AG9GENIChomozygous66076659
136782689967826900AT19GENIChomozygous66076662
136782868367828684TC19GENIChomozygous66076664
136782976967829770CA10GENIChomozygous66076670
136783005967830060CT11GENIChomozygous66076673
136783152967831530AG8GENIChomozygous66076676
136783270167832702GT11GENIChomozygous66076682