chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
47832031278320313CT16GENIChomozygous802695705
47832062078320621AC16GENIChomozygous802695706
47832129278321293CT21GENIChomozygous802695707
47832214078322141CT17GENIChomozygous802695708
47832291378322914TA17GENIChomozygous802695709
47832524978325250CT27GENICpossibly homozygous802695710
47832595578325956AG26GENIChomozygous802695711
47832624978326250GA20GENIChomozygous802695712
47832635778326358GA33GENIChomozygous802695713
47832674778326748CT22GENIChomozygous802695714
47832682978326830TC25GENIChomozygous802695715
47832703778327038TC18GENIChomozygous802695716
47832710578327106CA26GENICpossibly homozygous802695717