chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4100208662100208663TG71GENICpossibly homozygous112798360
4100209553100209554CT39GENIChomozygous112798362
4100209815100209816GA88GENIChomozygous112798364
4100212453100212454GT59GENICpossibly homozygous112798366
4100213631100213632AG46GENIChomozygous112798368
4100214547100214548CT54GENIChomozygous112798370
4100215137100215138TC75GENICpossibly homozygous112798372