chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
136780804367808044GA21GENIChomozygous66325643
136780850767808508CT13GENIChomozygous66325645
136780884767808848GA20GENIChomozygous66325647
136780920567809206GT19GENIChomozygous66325649
136780962067809621TC21GENIChomozygous66076610
136780991067809911AG23GENIChomozygous66076613
136781121267811213GT4GENIChomozygous66076621
136781123767811238AG4GENIChomozygous66076624
136781274967812750AT25GENIChomozygous66325653
136781343367813434TC15GENIChomozygous66325657
136781358667813587TC21GENIChomozygous66076627
136781479367814794AG28GENIChomozygous66325659
136781517567815176CT17GENIChomozygous66325661
136781668867816689GC8GENICpossibly homozygous66633947
136781682567816826CT15GENIChomozygous66325663
136781876167818762CG22GENIChomozygous66076633
136781975667819757GA22GENIChomozygous66325665
136782061967820620TC25GENIChomozygous66325667
136782257667822577TC25GENIChomozygous66076636
136782273767822738TC29GENIChomozygous66076639
136782299567822996AG19GENIChomozygous66076641
136782304667823047AC25GENIChomozygous66076644
136782304767823048GT24GENIChomozygous66076647
136782604967826050GA22GENIChomozygous66076656
136782650767826508AG30GENIChomozygous66076659
136782868367828684TC25GENIChomozygous66076664
136782976967829770CA19GENIChomozygous66076670
136783005967830060CT17GENIChomozygous66076673
136783152967831530AG15GENIChomozygous66076676
136783270167832702GT10GENIChomozygous66076682