chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108631468986314690CT29GENIChomozygous795100959
108631488886314889AG35GENIChomozygous795100960
108631736686317367GT36GENIChomozygous795100961
108632007386320074GT42GENIChomozygous795100962
108632117686321177AG32GENIChomozygous795100963
108632166286321663GA31GENIChomozygous795100964
108632189886321899TC33GENICheterozygous795100965
108632223486322235CT25GENIChomozygous795100966
108632232886322329CT33GENIChomozygous795100967
108632233386322334AG33GENIChomozygous795100968
108633105086331051AG44GENICpossibly homozygous795100969
108633257886332579GT37GENICpossibly homozygous795100970
108633422186334222GA28GENIChomozygous795100971