chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4157109368157109369CT17GENIChomozygous112905444
4157110290157110291AC21GENIChomozygous112905446
4157111333157111334GA28GENIChomozygous112905448
4157112730157112731CT24GENICpossibly homozygous112905450
4157114712157114713TC20GENIChomozygous112905452
4157117193157117194GA21GENIChomozygous112905454
4157117444157117445GA36GENIChomozygous112905456
4157120434157120435TG31GENIChomozygous112905460
4157120481157120482AG41GENIChomozygous112905462
4157120498157120499TG40GENIChomozygous112905464
4157120820157120821AT39GENIChomozygous112905466
4157121231157121232AG20GENIChomozygous112905468
4157121600157121601CT32GENIChomozygous112905470
4157121775157121776GT36GENIChomozygous112905472