| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:10455129-10455432 | Common:5; Rare:55; Clinvar:2; Clinvar (benign):6 | ||||
| chr11:10750697-10751038 | Common:4; Rare:92 | ||||
| chr11:10808836-10809202 | Common:3; Rare:158 | ||||
| chr11:10857300-10857383 | Rare:19 | ||||
| chr11:10858013-10858279 | Common:3; Rare:87 | ||||
| chr11:11621952-11622202 | Common:3; Rare:99 | ||||
| chr11:11841852-11842063 | Common:2; Rare:72 | ||||
| chr11:12377459-12377633 | Rare:69 | ||||
| chr11:13463164-13463336 | Common:1; Rare:64 | ||||
| chr11:13668342-13668765 | Common:1; Rare:138 | ||||
| chr11:14499779-14499918 | Common:2; Rare:49 | ||||
| chr11:14520314-14520549 | Rare:76 | ||||
| chr11:14643627-14643748 | Common:1; Rare:57 | ||||
| chr11:16738432-16738729 | Common:3; Rare:68 | ||||
| chr11:17207916-17208112 | Common:2; Rare:73 |