chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1169720380169720381TG19GENIChomozygous108753730
1169720427169720428GT23GENICpossibly homozygous108958102
1169720482169720483GC36GENICheterozygous109165657
1169720489169720490GA37GENICheterozygous109165659
1169720560169720561GA47GENICheterozygous108367913
1169720622169720623CT48GENICheterozygous108367917
1169720634169720635CA42GENICheterozygous108958104
1169720657169720658GA46GENICheterozygous108958106
1169720932169720933TG38GENICheterozygous109165663
1169721178169721179TA27GENICheterozygous109165665
1169721187169721188GA25GENICpossibly homozygous109165667
1169721405169721406GA16GENIChomozygous108367933