chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1171971646171971647CT14GENICpossibly homozygous108379727
1171971963171971964AG11GENIChomozygous108379731
1171972284171972285AG9GENIChomozygous108379733
1171972541171972542AG10GENIChomozygous108379739
1171973389171973390GA12GENIChomozygous108959901
1171975068171975069GA5GENIChomozygous108959902
1171975530171975531AG13GENIChomozygous108379749
1171977857171977858TA9GENIChomozygous108959903
1171978410171978411AT11GENIChomozygous108959904
1171979790171979791TC9GENIChomozygous108379757
1171980791171980792GA11GENIChomozygous108379763
1171980893171980894CT10GENIChomozygous108379765