chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
139368550593685506GT38GENIChomozygous114693511
139368550993685510GA38GENIChomozygous114428984
139368610493686105CA22GENIChomozygous114428986
139368778693687787CT26GENIChomozygous114428990
139368779893687799TA30GENIChomozygous114428992
139368796593687966CT23GENIChomozygous114428994
139368811493688115AC23GENIChomozygous114428998
139369095193690952GA25GENIChomozygous114429000
139369096093690961CT27GENIChomozygous114429002
139369177493691775AG25GENIChomozygous114429008
139369251093692511CT26GENIChomozygous114429010
139369309793693098CT24GENIChomozygous114429012
139369322093693221AG17GENIChomozygous114429014
139369616193696162TA5GENIChomozygous114650000
139369705893697059CA33GENIChomozygous114429016
139369707993697080GA29GENIChomozygous114429018
139369728193697282TG22GENIChomozygous114429020
139369734493697345CT18GENIChomozygous114429022
139369737293697373TC20GENIChomozygous114429024
139369832993698330GA17GENIChomozygous114429026
139369864193698642AG25GENIChomozygous114429028
139369978393699784TC26GENIChomozygous114429030
139370033793700338AG25GENIChomozygous114429032
139370062893700629GT25GENIChomozygous114429034
139370078193700782AG28GENIChomozygous114429036
139370079493700795TG28GENICpossibly homozygous114429038
139370266993702670CT31GENIChomozygous114429040
139370315793703158CT27GENIChomozygous114429042
139370451293704513CT16GENIChomozygous114429044
139370628893706289CA26GENIChomozygous114429046
139369118093691181AG22GENICheterozygous118466174
139369154893691549CG19GENICheterozygous118466175
139371047593710476AG23GENIChomozygous114429048
139371133993711340GA35GENIChomozygous114429050
139371436693714367AT24GENICpossibly homozygous114429052
139371436793714368AT24GENIChomozygous114429054