chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
12421864824218649TC14GENICpossibly homozygous108056616
12423768224237683GT14GENIChomozygous108056639
12424887324248874CA17GENIChomozygous108056647
12425452224254523CG26GENIChomozygous108056649
12425031424250315TG21GENICheterozygous108836675
12427574224275743AC11GENIChomozygous108056668
12427581224275813AG9GENIChomozygous108056669
12429515124295152GT15GENICheterozygous108056672
12429535924295360GT26GENIChomozygous108056673
12429541924295420GC23GENIChomozygous108056674
12429551524295516AT19GENIChomozygous108056675
12429569224295693GC17GENIChomozygous108056676
12429576424295765TG15GENIChomozygous108056677
12429577024295771CG14GENIChomozygous108056678
12429577324295774TG14GENIChomozygous108056679
12429578524295786GT19GENIChomozygous108056680
12429579624295797TG18GENIChomozygous108056681
12429582524295826TA17GENIChomozygous108056682
12429589524295896CA12GENIChomozygous108056683
12429773724297738AC13GENIChomozygous108056686
12429773924297740TC13GENIChomozygous108056687
12429775524297756TC13GENIChomozygous108056688