| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:14499590-14499872 | Common:2; Rare:96 | ||||
| chr11:14520041-14520525 | Common:1; Rare:137 | ||||
| chr11:14891621-14891680 | Rare:26 | ||||
| chr11:16607702-16607873 | Common:1; Rare:24 | ||||
| chr11:16738596-16738852 | Common:1; Rare:65 | ||||
| chr11:17074979-17075199 | Common:1; Rare:56 | ||||
| chr11:17077608-17077868 | Common:2; Rare:107 | ||||
| chr11:17207852-17208116 | Common:2; Rare:95 | ||||
| chr11:17276484-17276840 | Common:5; Rare:101; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr11:17295194-17295344 | Common:2; Rare:30 | ||||
| chr11:17310880-17311202 | Common:1; Rare:73 | ||||
| chr11:17311874-17312116 | Rare:53 | ||||
| chr11:17351493-17351813 | Common:1; Rare:68 | ||||
| chr11:17351912-17352022 | Common:1; Rare:25 | ||||
| chr11:18012985-18013058 | Common:3; Rare:25 |