chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1171971646171971647CT31GENIChomozygous108379727
1171971963171971964AG26GENIChomozygous108379731
1171972284171972285AG39GENIChomozygous108379733
1171972541171972542AG33GENIChomozygous108379739
1171973389171973390GA37GENIChomozygous108959901
1171974675171974676TG47GENICpossibly homozygous108379741
1171974722171974723TC22GENICheterozygous108379745
1171974752171974753AG15GENIChomozygous108379747
1171975068171975069GA43GENICpossibly homozygous108959902
1171975530171975531AG30GENIChomozygous108379749
1171977857171977858TA15GENIChomozygous108959903
1171978410171978411AT33GENICpossibly homozygous108959904
1171979790171979791TC31GENIChomozygous108379757
1171980791171980792GA34GENIChomozygous108379763
1171980893171980894CT46GENIChomozygous108379765