| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:10808870-10809104 | Common:1; Rare:101 | ||||
| chr11:10858002-10858260 | Common:3; Rare:85 | ||||
| chr11:11841938-11842063 | Common:1; Rare:37 | ||||
| chr11:13463150-13463361 | Common:1; Rare:76 | ||||
| chr11:13962654-13962809 | Common:1; Rare:39 | ||||
| chr11:16738450-16738717 | Common:3; Rare:60 | ||||
| chr11:17077568-17077880 | Common:3; Rare:137 | ||||
| chr11:17207911-17208082 | Common:2; Rare:65 | ||||
| chr11:18106055-18106308 | Common:2; Rare:67 | ||||
| chr11:18322086-18322347 | Common:6; Rare:101; Clinvar:2; Clinvar (benign):2 | ||||
| chr11:18322476-18322653 | Common:2; Rare:72 | ||||
| chr11:18394418-18394641 | Common:1; Rare:86; Clinvar (benign):1 | ||||
| chr11:18526841-18526971 | Rare:65 | ||||
| chr11:18588661-18588815 | Rare:57 | ||||
| chr11:18634332-18634590 | Common:2; Rare:83 |