chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4133689478133689479CT19GENICpossibly homozygous112833389
4133689677133689678AG36GENIChomozygous112833390
4133690178133690179AG75GENIChomozygous112833391
4133690184133690185GA74GENIChomozygous112833392
4133690728133690729TC30GENIChomozygous112833393