chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7130446765130446766CT21GENICpossibly homozygous116229555
7130451326130451327GA8GENICpossibly homozygous116229556
7130452094130452095GA20GENICpossibly homozygous116229557
7130452601130452602TC30GENIChomozygous115890250