chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104621730246217303GA4GENIChomozygous126488742
104622005846220059TC20GENIChomozygous116585259
104622010546220106TC19GENIChomozygous116585261
104622021846220219CG15GENIChomozygous116877618
104622116646221167CG25GENIChomozygous116877620
104622186946221870TC16GENICheterozygous117993470
104622200246222003TC18GENIChomozygous116585263
104622250646222507TC20GENIChomozygous116877622
104622254646222547GA21GENIChomozygous116877624
104622463546224636AG15GENIChomozygous116877628
104622477246224773AG5GENIChomozygous116877630
104622478846224789AC4GENIChomozygous116585267
104622502546225026AG18GENIChomozygous116877632
104622610746226108GA8GENIChomozygous116877634
104622618546226186CG21GENIChomozygous116877636
104622639346226394CT20GENIChomozygous116877638
104622689946226900AG14GENIChomozygous116585271
104622703046227031AT8GENIChomozygous116877640
104622802746228028AG13GENIChomozygous116585273
104622803046228031GC12GENIChomozygous116877642
104622850346228504TC17GENIChomozygous116877644
104623021946230220GA28GENIChomozygous116877646
104623217546232176TC20GENIChomozygous116877651
104623332746233328CT4GENIChomozygous118115378
104623356446233565TC26GENIChomozygous116877653
104623678046236781GC18GENIChomozygous126381901
104623988446239885AG16GENIChomozygous126381902
104623989846239899CG16GENIChomozygous126381903
104623992846239929AG11GENIChomozygous126381904
104623993046239931TG11GENIChomozygous126381905
104623996846239969CG10GENIChomozygous126488743
104623998646239987GC6GENIChomozygous126381906
104624052846240529AT8GENIChomozygous116585291
104624185846241859TC28GENIChomozygous116585293