chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5172490279172490280AG25GENIChomozygous876959722
5172495129172495130TC17GENIChomozygous876959723
5172497364172497365CT22GENIChomozygous876959724
5172500362172500363CT18GENIChomozygous876959725
5172501606172501607AC6GENIChomozygous876959726
5172501621172501622TC4GENIChomozygous876959727
5172501653172501654TC9GENIChomozygous876959728
5172502815172502816TG11GENIChomozygous876959729
5172502911172502912AT27GENIChomozygous876959730
5172502934172502935CT22GENIChomozygous876959731
5172505791172505792GA22GENIChomozygous876959732
5172506043172506044AG9GENIChomozygous876959733
5172506077172506078CT10GENIChomozygous876959734
5172513051172513052AG21GENIChomozygous876959735
5172514801172514802CT13GENIChomozygous876959736
5172514993172514994AG26GENIChomozygous876959737
5172515264172515265CT23GENIChomozygous876959738
5172515860172515861CT17GENIChomozygous876959739
5172516910172516911AC21GENIChomozygous876959740
5172518163172518164GA17GENIChomozygous876959741
5172518373172518374TC16GENIChomozygous876959742
5172519862172519863AC11GENIChomozygous876959743
5172521173172521174TG16GENIChomozygous876959744
5172525073172525074TC11GENIChomozygous876959745
5172525452172525453TC20GENIChomozygous876959746
5172526703172526704CT11GENIChomozygous876959747
5172527818172527819GT14GENIChomozygous876959748
5172528082172528083GT17GENIChomozygous876959749
5172528722172528723CT25GENIChomozygous876959750
5172531253172531254AG14GENIChomozygous876959751
5172532496172532497TC16GENIChomozygous876959752
5172538388172538389AC16GENIChomozygous876959753
5172542497172542498CG17GENIChomozygous876959754
5172543127172543128CT21GENIChomozygous876959755