| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:6390327-6390494 | Common:1; Rare:45 | ||||
| chr11:6481321-6481519 | Common:3; Rare:79 | ||||
| chr11:6603553-6603831 | Common:4; Rare:85; Clinvar (benign):3 | ||||
| chr11:6683286-6683399 | Common:2; Rare:55 | ||||
| chr11:8682628-8682816 | Common:2; Rare:85 | ||||
| chr11:10304818-10305083 | Common:1; Rare:59 | ||||
| chr11:10858023-10858269 | Common:2; Rare:78 | ||||
| chr11:11841859-11842016 | Common:2; Rare:61 | ||||
| chr11:14520318-14520549 | Rare:74 | ||||
| chr11:16738466-16738687 | Common:2; Rare:44 | ||||
| chr11:17077618-17077877 | Common:2; Rare:110 | ||||
| chr11:17207920-17208111 | Common:1; Rare:72 | ||||
| chr11:18322491-18322582 | Common:2; Rare:40 | ||||
| chr11:18526935-18526987 | Rare:19 | ||||
| chr11:27506752-27506842 | Common:1; Rare:40 |