| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:13009127-13009343 | Common:2; Rare:79 | ||||
| chr11:13463119-13463389 | Common:1; Rare:100 | ||||
| chr11:14643631-14643743 | Common:1; Rare:54 | ||||
| chr11:14892187-14892262 | Rare:39 | ||||
| chr11:16738444-16738769 | Common:3; Rare:74 | ||||
| chr11:17013838-17013987 | Common:6; Rare:60 | ||||
| chr11:17014254-17014326 | Rare:26 | ||||
| chr11:17077583-17077899 | Common:2; Rare:137 | ||||
| chr11:17207905-17208102 | Common:2; Rare:77 | ||||
| chr11:17276458-17276828 | Common:5; Rare:105; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr11:18012896-18013248 | Common:6; Rare:118 | ||||
| chr11:18106037-18106308 | Common:2; Rare:83 | ||||
| chr11:18248601-18248910 | Common:1; Rare:74 | ||||
| chr11:18266063-18266313 | Common:3; Rare:50 | ||||
| chr11:18322075-18322342 | Common:5; Rare:102; Clinvar:2; Clinvar (benign):2 |