chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
47832031278320313CT23GENIChomozygous952180947
47832062078320621AC28GENICpossibly homozygous952180948
47832129278321293CT18GENIChomozygous952180949
47832214078322141CT22GENIChomozygous952180950
47832291378322914TA8GENIChomozygous952180951
47832524978325250CT29GENIChomozygous952180952
47832595578325956AG33GENIChomozygous952180953
47832624978326250GA32GENIChomozygous952180954
47832635778326358GA26GENIChomozygous952180955
47832674778326748CT25GENIChomozygous952180956
47832682978326830TC25GENIChomozygous952180957
47832703778327038TC18GENIChomozygous952180958
47832710578327106CA23GENIChomozygous952180959