chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
145961122959611245GTGTGTGTGTGTGCGC32GENICpossibly homozygous129164488
145961672959616769TCTCTCGCTCTCTCGCTCTCTCGCTCTCTCGCTCTCTCGC11GENIChomozygous129164489
145961623159616232AG43GENIChomozygous113473275
145961630059616301AC27GENIChomozygous113473277
145961753959617540C53GENIChomozygous129164490
145961971359619714CT77GENIChomozygous113473279