Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:27506748-27506875 | Common:1; Rare:53 | ||||
chr11:28108091-28108443 | Common:2; Rare:105 | ||||
chr11:30322971-30323164 | Common:1; Rare:55 | ||||
chr11:31369735-31369882 | Rare:45 | ||||
chr11:31509575-31509790 | Common:1; Rare:67 | ||||
chr11:32091404-32091449 | Rare:11 | ||||
chr11:32583663-32583918 | Rare:93 | ||||
chr11:33161449-33161682 | Common:6; Rare:65 | ||||
chr11:33257204-33257427 | Common:3; Rare:74 | ||||
chr11:33722627-33722844 | Common:2; Rare:44 | ||||
chr11:33736375-33736605 | Common:2; Rare:72 | ||||
chr11:33774484-33774686 | Common:2; Rare:72 | ||||
chr11:34105481-34105719 | Common:2; Rare:78 | ||||
chr11:34916292-34916681 | Common:10; Rare:158; Clinvar:5; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
chr11:35617729-35617999 | Rare:62 |