chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5172490279172490280AG16GENIChomozygous886370083
5172495129172495130TC16GENIChomozygous886370084
5172497364172497365CT26GENIChomozygous886370085
5172500362172500363CT8GENIChomozygous886370086
5172501606172501607AC4GENIChomozygous886370087
5172501653172501654TC11GENIChomozygous886370088
5172502815172502816TG4GENIChomozygous886370089
5172502911172502912AT13GENIChomozygous886370090
5172502934172502935CT14GENIChomozygous886370091
5172505791172505792GA26GENIChomozygous886370092
5172506043172506044AG8GENIChomozygous886370093
5172506077172506078CT10GENIChomozygous886370094
5172513051172513052AG14GENIChomozygous886370095
5172514801172514802CT10GENIChomozygous886370096
5172514993172514994AG18GENIChomozygous886370097
5172515264172515265CT20GENIChomozygous886370098
5172515860172515861CT16GENIChomozygous886370099
5172516910172516911AC10GENIChomozygous886370100
5172518163172518164GA10GENIChomozygous886370101
5172518373172518374TC10GENIChomozygous886370102
5172521173172521174TG13GENIChomozygous886370103
5172525073172525074TC4GENIChomozygous886370104
5172525452172525453TC19GENIChomozygous886370105
5172526703172526704CT9GENIChomozygous886370106
5172527818172527819GT11GENIChomozygous886370107
5172528082172528083GT16GENIChomozygous886370108
5172528722172528723CT9GENIChomozygous886370109
5172531253172531254AG5GENIChomozygous886370110
5172532496172532497TC7GENIChomozygous886370111
5172535664172535665AC4GENIChomozygous886370112
5172538388172538389AC14GENIChomozygous886370113
5172542497172542498CG16GENIChomozygous886370114