chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1140522364140522365AG27GENIChomozygous108257671
1140526614140526615TC26GENIChomozygous108257685
1140527335140527336GA7GENIChomozygous109144202
1140525551140525552CT23GENIChomozygous109144192
1140525930140525931AG20GENIChomozygous109144198
1140526889140526890CT20GENIChomozygous109144200
1140527350140527351TG8GENIChomozygous108257687
1140527743140527744GA31GENIChomozygous109144204
1140529184140529185CA19GENIChomozygous109144205
1140529227140529228AG27GENIChomozygous109144207
1140529336140529337CT18GENIChomozygous109144209
1140529888140529889TC17GENIChomozygous109144211
1140530270140530271AG28GENIChomozygous109144213
1140530613140530614CT15GENIChomozygous109144215
1140530686140530687CG12GENIChomozygous109144217
1140532859140532860CT20GENIChomozygous109144221
1140533188140533189AG22GENIChomozygous108257697
1140533256140533257CA28GENIChomozygous109144223
1140529297140529298AT19GENIChomozygous120486519
1140530808140530809AT11GENIChomozygous120486520
1140530813140530814TG12GENIChomozygous120486521
1140531559140531560TA17GENIChomozygous120486522
1140531560140531561CT18GENIChomozygous120486523
1140535366140535367AT35GENIChomozygous109144229