chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
143455563234555633TC54GENIChomozygous113419762
143455592934555930AC52GENIChomozygous113419765
143455646634556467AT32GENIChomozygous113419766
143455708034557081CT57GENIChomozygous113419767
143455755534557556GA47GENIChomozygous131931306
143455778034557781TC17GENIChomozygous113419768
143455791334557914TC31GENIChomozygous131931307
143455814834558149GA51GENIChomozygous113419769
143455828134558282TC53GENIChomozygous113419770
143455858934558590CT46GENIChomozygous113419771
143455912534559126GA46GENIChomozygous113419772
143455989034559891CT28GENIChomozygous113419774
143455989134559892TG28GENIChomozygous113419775
143455992434559924T20GENICpossibly homozygous130426113
143456077334560774CT48GENIChomozygous131931308
143456120934561210CT46GENIChomozygous131931309
143456170334561704CT54GENIChomozygous131931310
143456233234562333AG44GENIChomozygous113419777
143456291234562912AG19GENICheterozygous131928575
143455789134557891G29GENIChomozygous131928573
143455789434557894GGG27GENIChomozygous131928574
143455792434557924T31GENIChomozygous129144859
143456692434566924AC42GENIChomozygous129144862
143456713634567137TC45GENIChomozygous131931311
143456775734567758GA45GENIChomozygous113419778
143456854734568548TC49GENIChomozygous113419779
143456880334568804CG38GENIChomozygous113419780
143456911134569112AG51GENIChomozygous113419781