| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:130547102-130547228 | Common:2; Rare:32 | ||||
| chr11:131067441-131067601 | Rare:36 | ||||
| chr11:131186863-131186968 | Common:2; Rare:21 | ||||
| chr11:131540627-131540978 | Common:2; Rare:65 | ||||
| chr11:131722735-131722885 | Rare:23 | ||||
| chr11:133064540-133064725 | Common:2; Rare:42 | ||||
| chr11:133109340-133109518 | Rare:45 | ||||
| chr11:133337369-133337462 | Common:3; Rare:20 | ||||
| chr11:133783141-133783234 | Common:4; Rare:22 | ||||
| chr11:134037347-134037443 | Rare:34 | ||||
| chr11:134051001-134051110 | Common:3; Rare:56 | ||||
| chr11:134143992-134144392 | Common:4; Rare:128; Clinvar (pathogenic):1 | ||||
| chr11:134145677-134146008 | Common:1; Rare:79; Clinvar (pathogenic):1 | ||||
| chr11:134148314-134148669 | Rare:125 | ||||
| chr11:134148876-134149194 | Common:11; Rare:117 |