chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7144606485144606486TC50GENIChomozygous115945524
7144606678144606679AC54GENIChomozygous115945526
7144606686144606687GA48GENIChomozygous115945527
7144606730144606731CT56GENIChomozygous115945529
7144606792144606795TTG53GENIChomozygous128531955
7144606801144606801GC51GENIChomozygous128531956
7144607621144607621T56GENICpossibly homozygous128531957