chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3154514251154514255CGGC----6GENIChomozygous698853096
3154514276154514277TG11GENIChomozygous546876713
3154514414154514415AAGTCT5GENIChomozygous698853098
3154514475154514476TC7GENIChomozygous546876714
3154514477154514478TC8GENIChomozygous546876715
3154515475154515476GA18GENIChomozygous546876716
3154515681154515682TA18GENICheterozygous546876717
3154516008154516009GA8GENICpossibly homozygous546876718
3154516009154516010AT8GENICpossibly homozygous546876719
3154516260154516261TC4GENIChomozygous546876720
3154516884154516885AG17GENICpossibly homozygous546876721
3154517077154517078TC14GENIChomozygous548345073
3154517156154517157AG19GENICpossibly homozygous546876722
3154517593154517594TC11GENICpossibly homozygous546876723
3154517632154517633G-10GENICheterozygous698853099
3154517898154517899TC16GENIChomozygous546876724
3154517982154517986GGCA----9GENICheterozygous698853100
3154518068154518069GA15GENIChomozygous546876725
3154518158154518159TTA18GENIChomozygous698853101
3154518562154518563CT22GENIChomozygous548345074
3154518737154518738AG14GENIChomozygous546876726
3154519100154519101CT26GENICpossibly homozygous548345075
3154519184154519185CCA1GENIChomozygous698853102
3154519315154519316CT12GENIChomozygous546876727
3154519985154519986AG9GENICpossibly homozygous546876728
3154520058154520059TC16GENIChomozygous546876729
3154520781154520782TC13GENIChomozygous546876730
3154520987154520988CT18GENICpossibly homozygous546876731
3154522134154522135AG17GENIChomozygous546876732