chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4157109368157109369CT24GENIChomozygous112905444
4157110048157110048GC14GENIChomozygous128096015
4157110290157110291AC22GENIChomozygous112905446
4157111333157111334GA19GENIChomozygous112905448
4157112692157112692AC12GENIChomozygous128096016
4157112730157112731CT13GENIChomozygous112905450
4157113732157113733A26GENIChomozygous128096017
4157113735157113737AA27GENIChomozygous128096018
4157114712157114713TC23GENIChomozygous112905452
4157117020157117020CTAGCAGTTATTCTCTTTGC15GENIChomozygous128096019
4157117193157117194GA20GENIChomozygous112905454
4157117444157117445GA23GENIChomozygous112905456
4157117565157117565ACACACACACAT7GENIChomozygous128096020
4157117641157117643CT8GENICheterozygous130939735
4157118236157118236T18GENIChomozygous128096022
4157119153157119154C13GENIChomozygous128096023
4157120342157120342A18GENIChomozygous128096024
4157120434157120435TG20GENIChomozygous112905460
4157120481157120482AG23GENIChomozygous112905462
4157120498157120499TG20GENIChomozygous112905464
4157120820157120821AT12GENIChomozygous112905466
4157121231157121232AG31GENIChomozygous112905468
4157121262157121262C34GENIChomozygous128096025
4157121600157121601CT19GENIChomozygous112905470
4157121775157121776GT30GENIChomozygous112905472