chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5133865059133865060CA53GENIChomozygous114531697
5133873262133873263AG33GENIChomozygous114015138
5133869655133869656AG30GENIChomozygous114015135
5133869866133869867GA49GENIChomozygous114015136
5133871296133871297TG55GENIChomozygous114015137
5133873933133873934CT43GENIChomozygous114531699
5133874216133874217AT50GENICpossibly homozygous114531701
5133875581133875582AG47GENIChomozygous114015140
5133876277133876278AT38GENIChomozygous114015142
5133878399133878400GA37GENIChomozygous114531703
5133874953133874957GACA29GENIChomozygous128241327