| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:16791715-16791921 | Common:2; Rare:31 | ||||
| chr11:17013711-17014099 | Common:11; Rare:170 | ||||
| chr11:17077616-17078118 | Common:4; Rare:183 | ||||
| chr11:17207900-17208170 | Common:2; Rare:108 | ||||
| chr11:17208344-17208548 | Rare:37 | ||||
| chr11:17276442-17276794 | Common:4; Rare:99; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr11:17389259-17389510 | Common:2; Rare:45 | ||||
| chr11:17389652-17389794 | Rare:37 | ||||
| chr11:17407620-17407900 | Common:1; Rare:44 | ||||
| chr11:17544348-17544548 | Common:4; Rare:49; Clinvar:2 | ||||
| chr11:17734520-17734810 | Common:4; Rare:88 | ||||
| chr11:18012894-18013285 | Common:6; Rare:133 | ||||
| chr11:18106039-18106172 | Common:1; Rare:56 | ||||
| chr11:18322071-18322354 | Common:6; Rare:105; Clinvar:2; Clinvar (benign):2 | ||||
| chr11:18322370-18322690 | Common:2; Rare:103 |