chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6144512102144512104TA--2GENICheterozygous54762785
6144512667144512668CT11GENICheterozygous54762786
6144512950144512951GA18GENIChomozygous54762787
6144514714144514715AG23GENICheterozygous54762788
6144515833144515834TC9GENIChomozygous54762792
6144516170144516171AG16GENICpossibly homozygous54762793
6144518272144518273AT16GENIChomozygous54762794
6144518417144518418CCG14GENIChomozygous54762795
6144518607144518608GT28GENIChomozygous54762796
6144518869144518870CA8GENIChomozygous54762797
6144520045144520046AT13GENIChomozygous54762798
6144520062144520063CT19GENIChomozygous54762799
6144520151144520152TC19GENICpossibly homozygous54762800
6144520363144520364CG9GENIChomozygous54762801
6144520499144520502CCC---2GENIChomozygous54762802
6144520883144520884CCA9GENIChomozygous54762803
6144520887144520888CCT6GENIChomozygous54762804
6144520916144520917GA4GENIChomozygous54762805
6144523383144523384TC10GENIChomozygous54762807