chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108633779286337792G12GENIChomozygous128841889
108633781286337813T13GENIChomozygous128841890
108633781486337815A13GENIChomozygous128841891
108633782386337823C16GENIChomozygous128841892
108633787386337873C16GENIChomozygous128841893
108633789586337896G16GENIChomozygous128841894
108633789886337899G16GENIChomozygous128841895
108633790986337910TC16GENIChomozygous116667452
108633791086337911GT17GENIChomozygous116667454
108633794386337943A15GENIChomozygous128841896
108633797386337974AC13GENIChomozygous116667456
108633798086337981AC15GENIChomozygous116667458
108633803186338032A16GENIChomozygous128841897
108633805286338052C22GENIChomozygous128841898
108633805386338053C22GENIChomozygous128841899
108633808486338085G25GENIChomozygous128841900
108633810886338110CC23GENIChomozygous128841901
108633814286338142G21GENIChomozygous128841902
108633816686338166T22GENIChomozygous128841903
108633817186338171A22GENIChomozygous128841904
108633819086338190C20GENIChomozygous128841905
108633821286338212GG15GENIChomozygous128841906
108633823686338236A17GENIChomozygous128841907
108633831786338317G20GENIChomozygous128841908
108633832986338330A19GENIChomozygous128841909
108633833386338333C19GENIChomozygous128841910
108633834086338340G18GENIChomozygous128841911
108633835086338350G21GENIChomozygous128841912
108633835486338355AC20GENIChomozygous116667460
108633836786338368G22GENIChomozygous128841913
108633837186338372TG20GENIChomozygous116816133
108633837686338377T22GENIChomozygous128841914
108633838786338387C22GENIChomozygous128841915