chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5172490279172490280AG31GENIChomozygous958099818
5172497364172497365CT31GENIChomozygous958099819
5172499346172499347GA47GENIChomozygous958099820
5172500362172500363CT41GENIChomozygous958099821
5172501606172501607AC26GENIChomozygous958099822
5172502815172502816TG19GENIChomozygous958099823
5172502911172502912AT25GENICpossibly homozygous958099824
5172502934172502935CT27GENIChomozygous958099825
5172505791172505792GA38GENIChomozygous958099826
5172506077172506078CT47GENIChomozygous958099827
5172514801172514802CT37GENICpossibly homozygous958099828
5172514993172514994AG38GENIChomozygous958099829
5172515264172515265CT35GENIChomozygous958099830
5172515860172515861CT31GENIChomozygous958099831
5172516910172516911AC27GENIChomozygous958099832
5172518163172518164GA32GENICpossibly homozygous958099833
5172518373172518374TC40GENIChomozygous958099834
5172519862172519863AC17GENIChomozygous958099835
5172525073172525074TC28GENIChomozygous958099836
5172525452172525453TC20GENIChomozygous958099837
5172526703172526704CT16GENIChomozygous958099838
5172527818172527819GT26GENIChomozygous958099839
5172528082172528083GT16GENIChomozygous958099840
5172528722172528723CT29INTERGENIChomozygous958099841
5172531253172531254AG19INTERGENIChomozygous958099842
5172532496172532497TC28INTERGENIChomozygous958099843
5172538388172538389AC31INTERGENIChomozygous958099844
5172539936172539937CT28INTERGENIChomozygous958099845
5172542099172542100AG11INTERGENICheterozygous958099846
5172542100172542101CT11INTERGENICheterozygous958099847
5172542497172542498CG18INTERGENIChomozygous958099848
5172543127172543128CT13INTERGENIChomozygous958099849