chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4169645649169645650CT28GENIChomozygous119538283
4169773450169773451AC33GENIChomozygous113406610
4169775789169775790TC50GENIChomozygous113406612
4169778408169778409TC41GENIChomozygous113406614
4169778739169778740AG13GENIChomozygous113406616
4169778966169778967TC43GENIChomozygous113406618
4169779116169779117AG25GENIChomozygous113406620
4169797508169797509GA44GENIChomozygous113406626
4169798341169798342TC18GENIChomozygous113406628
4169798966169798967CA34GENICpossibly homozygous113406630
4169799587169799588CT39GENIChomozygous113406632
4169799820169799821CT6GENIChomozygous113406634
4169799917169799918AC27GENIChomozygous113313973
4169799963169799964CT55GENIChomozygous113313974
4169804815169804816GA32GENIChomozygous113313975
4169808853169808854AG15GENIChomozygous113313977
4169809047169809048TC55GENIChomozygous113313978
4169811111169811112CT24GENIChomozygous113313980
4169845397169845398GT12GENIChomozygous112946694
4169873955169873956GA17GENIChomozygous119550857
4169893886169893887CA20GENIChomozygous112947012
4169990682169990683CT34GENIChomozygous119320453