chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
184058708940587090TG14GENIChomozygous110329492
184058716340587164CT20GENIChomozygous110329494
184058787240587873GA19GENIChomozygous110589678
184058861240588613CA30GENIChomozygous110329496
184059019440590195GA23GENIChomozygous110329498
184059168940591690GC25GENIChomozygous110329500
184059322940593230CT13GENIChomozygous119490608
184059325540593256GA6GENIChomozygous119490609
184059325940593260AG5GENIChomozygous119490610
184059420140594202CT24GENIChomozygous110329502
184059421540594216CG23GENIChomozygous110329504
184059545040595451GA27GENIChomozygous110329506
184059572540595726AG15GENIChomozygous110463648
184059600440596005AG14GENIChomozygous110329508
184059746140597462TG28GENIChomozygous110329510
184059783640597837AG18GENIChomozygous110329512