| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:6619178-6619539 | Common:2; Rare:132; Clinvar:4; Clinvar (benign):14; Clinvar (pathogenic):2 | ||||
| chr11:6683187-6683644 | Common:6; Rare:173 | ||||
| chr11:7020301-7020502 | Rare:69 | ||||
| chr11:7485227-7485539 | Rare:58 | ||||
| chr11:7513626-7514050 | Common:6; Rare:126 | ||||
| chr11:7577412-7577597 | Rare:39 | ||||
| chr11:7597147-7597224 | Common:2; Rare:13 | ||||
| chr11:7597312-7597637 | Common:1; Rare:93 | ||||
| chr11:7673442-7673576 | Common:1; Rare:45 | ||||
| chr11:8168985-8169064 | Common:2; Rare:30 | ||||
| chr11:8682628-8682816 | Common:2; Rare:85 | ||||
| chr11:8682928-8683269 | Common:2; Rare:114 | ||||
| chr11:8717764-8718184 | Common:7; Rare:115 | ||||
| chr11:8870954-8871343 | Common:2; Rare:94 | ||||
| chr11:8910921-8911265 | Common:6; Rare:94 |