chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10109665880109665881AG53GENIChomozygous116718979
10109666101109666102GT40GENICpossibly homozygous116718981
10109666133109666134TC47GENIChomozygous116718983
10109666295109666296GT40GENIChomozygous116718985
10109666391109666392CT32GENIChomozygous116718987
10109667406109667407AG40GENIChomozygous116718989
10109668367109668368TC58GENIChomozygous116718991
10109672473109672474CT45GENIChomozygous116718993
10109674110109674111AG44GENIChomozygous116718995
10109674118109674118G45GENIChomozygous128860702