chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
136780804367808044GA37GENICpossibly homozygous66325643
136780850767808508CT30GENIChomozygous66325645
136780884767808848GA24GENIChomozygous66325647
136780920567809206GT18GENIChomozygous66325649
136780962067809621TC25GENIChomozygous66076610
136780991067809911AG14GENIChomozygous66076613
136781274967812750AT31GENIChomozygous66325653
136781343367813434TC15GENIChomozygous66325657
136781358667813587TC17GENIChomozygous66076627
136781479367814794AG36GENIChomozygous66325659
136781517567815176CT22GENIChomozygous66325661
136781668867816689GC7GENIChomozygous66633947
136781682567816826CT14GENIChomozygous66325663
136781876167818762CG25GENIChomozygous66076633
136781975667819757GA27GENIChomozygous66325665
136782061967820620TC22GENIChomozygous66325667
136782257667822577TC24GENIChomozygous66076636
136782273767822738TC32GENIChomozygous66076639
136782299567822996AG31GENIChomozygous66076641
136782304667823047AC20GENIChomozygous66076644
136782304767823048GT20GENIChomozygous66076647
136782604967826050GA18GENIChomozygous66076656
136782650767826508AG36GENIChomozygous66076659
136782868367828684TC21GENIChomozygous66076664
136782976967829770CA28GENIChomozygous66076670
136783005967830060CT23GENIChomozygous66076673
136783152967831530AG20GENIChomozygous66076676
136783270167832702GT18GENICpossibly homozygous66076682