chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
12941348729413488GC29GENIChomozygous109069679
12941366929413670GA27GENIChomozygous109069681
12941372929413730AG36GENIChomozygous108705640
12941377829413779CT31GENIChomozygous109069683
12941381529413816AG36GENIChomozygous109069685
12941386529413866GA40GENIChomozygous109069687
12941391329413914CT43GENIChomozygous109069689
12941397929413980TG34GENIChomozygous109069691
12941411829414119GT20GENIChomozygous108705646
12941483729414838CA18GENIChomozygous109069693
12941507229415073GA15GENIChomozygous109069695
12941517929415180GT20GENIChomozygous108705654
12941522629415227GA28GENIChomozygous109069697
12941542829415429GA29GENIChomozygous109069699
12941593029415931AG22GENIChomozygous108705656
12941598429415985TC22GENIChomozygous109069701
12941644429416445GA18GENIChomozygous108705660
12941740729417408CT25GENIChomozygous108705666
12941765529417656AT18GENIChomozygous108705668
12941771629417717TG22GENIChomozygous108705670
12941812429418125AG16GENIChomozygous108705672
12941823129418232TC18GENIChomozygous108705674
12941829029418291GA16GENIChomozygous108705676
12941865129418652TC16GENIChomozygous108705678
12941869129418692TG21GENIChomozygous108705680
12941873129418732GT17GENIChomozygous108705682
12941885029418851CT20GENIChomozygous109069703
12941902629419027AC31GENIChomozygous108705684
12941917329419174GA24GENIChomozygous108705686
12941942129419422TC15GENIChomozygous108705688
12941978729419788CA30GENIChomozygous108705690
12942008329420084TC18GENIChomozygous109069707
12942015229420153TC18GENIChomozygous108705692
12942023529420236CT22GENIChomozygous108705694
12942024929420250AC26GENIChomozygous108705696
12942040629420407CT29GENIChomozygous108705698
12942041529420416AG32GENIChomozygous108705700
12942164029421641AG26GENIChomozygous109069709
12942259529422596TA27GENIChomozygous108705708
12942262929422630GT12GENIChomozygous108705710