chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4145264840145264841TC19INTERGENICheterozygous56967032
4145264959145264960GT18INTERGENIChomozygous56967033
4145265203145265204TC18INTERGENICheterozygous56967035
4145265514145265515AT21INTERGENICheterozygous57343335
4145266273145266274AG23INTERGENIChomozygous56967036
4145267253145267254CG18INTERGENICheterozygous56967038
4145268434145268435GA14INTERGENICheterozygous57343339
4145268861145268862AC8INTERGENIChomozygous56967039
4145269747145269748GA9INTERGENIChomozygous56967041
4145270099145270100GT11INTERGENICheterozygous57343343
4145270144145270145GA12INTERGENICheterozygous58083813
4145270152145270153CT13INTERGENICheterozygous56967042
4145270333145270334G-12INTERGENICheterozygous58083814
4145270876145270877TTACAC13INTERGENICheterozygous58083815
4145270880145270881CT14INTERGENICheterozygous56967046
4145271000145271001CT16INTERGENICheterozygous58083816
4145271825145271826AC13INTERGENICheterozygous56967047
4145272280145272281CT20INTERGENICheterozygous56967048
4145272496145272497TC20INTERGENIChomozygous56967049
4145273041145273042GA17INTERGENICheterozygous56967051
4145274093145274094CT12INTERGENIChomozygous56967052
4145274314145274315GA16INTERGENICheterozygous58083817
4145274448145274449T-15INTERGENICheterozygous56967053
4145274543145274544TC18INTERGENICheterozygous56967054
4145275064145275065AG16INTERGENICheterozygous58083818
4145275203145275204GT9INTERGENIChomozygous56967055
4145275573145275574GA14INTERGENICheterozygous57512284
4145275740145275741TC16INTERGENIChomozygous56967058
4145275773145275774TTG19INTERGENIChomozygous56967059
4145275795145275796AG22INTERGENIChomozygous56967060
4145275822145275823AG28INTERGENIChomozygous56967061
4145275838145275839AG25INTERGENIChomozygous56967062
4145277100145277101TC22INTERGENIChomozygous56967063
4145277365145277366AC15INTERGENIChomozygous56967064
4145277647145277648TC13INTERGENIChomozygous56967065
4145280486145280487CG13INTERGENIChomozygous56967068