| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:17276607-17276827 | Common:3; Rare:57; Clinvar:3 | ||||
| chr11:18106037-18106308 | Common:2; Rare:83 | ||||
| chr11:18322119-18322317 | Common:3; Rare:75; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:18322491-18322629 | Common:2; Rare:60 | ||||
| chr11:18394331-18394633 | Common:1; Rare:120; Clinvar (benign):1 | ||||
| chr11:18526812-18527008 | Common:1; Rare:92 | ||||
| chr11:18588667-18588838 | Common:2; Rare:56 | ||||
| chr11:18634332-18634566 | Common:2; Rare:74 | ||||
| chr11:18634811-18634874 | Rare:6 | ||||
| chr11:19116934-19117203 | Common:3; Rare:71 | ||||
| chr11:20364094-20364181 | Rare:22 | ||||
| chr11:20387475-20387765 | Common:5; Rare:94 | ||||
| chr11:22625522-22625601 | Rare:38; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr11:22625813-22626002 | Common:2; Rare:64; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:27506721-27506875 | Common:1; Rare:72 |