chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2233603310233603311CT18GENIChomozygous110310891
2233603332233603333CA14GENIChomozygous110310893
2233603349233603350CG11GENIChomozygous110310895
2233603393233603394AG14GENIChomozygous110310897
2233603542233603543GA12GENIChomozygous120219970
2233604448233604449AG34GENIChomozygous110310899
2233605147233605148GC18GENIChomozygous110310901
2233608357233608358TA16GENICpossibly homozygous120326362
2233608799233608800GA13GENIChomozygous120326363
2233609230233609231TA7GENIChomozygous110310913
2233610088233610089CT26GENIChomozygous110310915
2233610551233610552CG24GENIChomozygous120326364
2233612250233612251GA30GENIChomozygous110310917
2233613195233613196AG22GENIChomozygous110310919
2233613635233613636GT25GENIChomozygous110310921
2233613661233613662CG25GENIChomozygous110310923
2233614061233614062CA13GENIChomozygous110310925
2233615830233615831CT17GENIChomozygous110310927
2233616021233616022AG9GENIChomozygous110310929
2233616914233616915GA17GENIChomozygous120326365
2233617390233617391AG5GENIChomozygous110310931
2233617474233617475GA7GENIChomozygous110310933
2233619256233619257TC20GENICpossibly homozygous120326366