chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5157759657157759658CG28GENICpossibly homozygous114070442
5157761571157761572CT46GENIChomozygous114070443
5157766191157766192AG42GENIChomozygous114070444
5157766624157766625GC31GENIChomozygous114070445