chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
47832062078320621AC21GENICpossibly homozygous996783157
47832319078323191CT28GENIChomozygous996783158
47832323978323240TC25GENIChomozygous996783159
47832524978325250CT30GENIChomozygous996783160
47832595578325956AG37GENIChomozygous996783161