| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:117144015-117144981 | Common:58; Rare:1175 | ||||
| chr11:117178301-117179264 | Common:15; Rare:664 | ||||
| chr11:117179582-117180444 | Common:8; Rare:322 | ||||
| chr11:117181251-117181604 | Common:3; Rare:110 | ||||
| chr11:117220004-117220404 | Rare:114 | ||||
| chr11:117231427-117231827 | Common:8; Rare:74 | ||||
| chr11:117231920-117232220 | Common:2; Rare:249 | ||||
| chr11:117232240-117232430 | Rare:32 | ||||
| chr11:117232450-117232900 | Common:16; Rare:562 | ||||
| chr11:117327558-117328001 | Common:9; Rare:331 | ||||
| chr11:117328082-117328207 | Rare:39 | ||||
| chr11:117328412-117328812 | Common:3; Rare:82 | ||||
| chr11:117828620-117829250 | Common:6; Rare:131 | ||||
| chr11:117986149-117986549 | Common:26; Rare:462; Clinvar:14; Clinvar (benign):3 | ||||
| chr11:118102501-118103253 | Common:35; Rare:349 |