chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108633779286337792G17GENIChomozygous128841889
108633781286337813T17GENIChomozygous128841890
108633781486337815A18GENIChomozygous128841891
108633782386337823C17GENIChomozygous128841892
108633787386337873C10GENIChomozygous128841893
108633789586337896G10GENIChomozygous128841894
108633789886337899G11GENIChomozygous128841895
108633790986337910TC12GENIChomozygous116667452
108633791086337911GT12GENIChomozygous116667454
108633794386337943A9GENIChomozygous128841896
108633797386337974AC11GENIChomozygous116667456
108633798086337981AC12GENIChomozygous116667458
108633803186338032A17GENIChomozygous128841897
108633805286338052C16GENIChomozygous128841898
108633805386338053C16GENIChomozygous128841899
108633808486338085G22GENIChomozygous128841900
108633810886338110CC26GENIChomozygous128841901
108633814286338142G26GENIChomozygous128841902
108633816686338166T27GENIChomozygous128841903
108633817186338171A27GENIChomozygous128841904
108633819086338190C27GENIChomozygous128841905
108633821286338212GG22GENIChomozygous128841906
108633823686338236A22GENIChomozygous128841907
108633831786338317G17GENIChomozygous128841908
108633832986338330A17GENIChomozygous128841909
108633833386338333C17GENIChomozygous128841910
108633834086338340G18GENIChomozygous128841911
108633835086338350G19GENIChomozygous128841912
108633835486338355AC19GENIChomozygous116667460
108633836786338368G19GENIChomozygous128841913
108633837186338372TG16GENIChomozygous116816133
108633837686338377T15GENIChomozygous128841914
108633838786338387C15GENIChomozygous128841915