| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:18322107-18322306 | Common:3; Rare:74; Clinvar:2; Clinvar (benign):2 | ||||
| chr11:18322462-18322605 | Common:2; Rare:61 | ||||
| chr11:18526825-18527016 | Common:1; Rare:93 | ||||
| chr11:18588639-18588791 | Rare:60 | ||||
| chr11:18634291-18634563 | Common:3; Rare:92 | ||||
| chr11:19714077-19714195 | Rare:26 | ||||
| chr11:22625803-22625985 | Common:2; Rare:64; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr11:27506718-27506875 | Common:1; Rare:74 | ||||
| chr11:28108101-28108421 | Common:1; Rare:96 | ||||
| chr11:31369737-31369911 | Rare:53 | ||||
| chr11:31509586-31509787 | Common:1; Rare:62 | ||||
| chr11:32091245-32091413 | Rare:60 | ||||
| chr11:33015784-33015946 | Common:1; Rare:63 | ||||
| chr11:33161398-33161635 | Common:6; Rare:61 | ||||
| chr11:33736387-33736583 | Common:2; Rare:63 |