chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7144606485144606486TC57GENIChomozygous115945524
7144606678144606679AC52GENIChomozygous115945526
7144606686144606687GA53GENIChomozygous115945527
7144606730144606731CT42GENIChomozygous115945529
7144606792144606795TTG42GENIChomozygous128531955
7144606801144606801GC43GENIChomozygous128531956
7144607621144607621T37GENICpossibly homozygous128531957