| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:8964916-8965034 | Common:1; Rare:28 | ||||
| chr11:9003985-9004197 | Common:1; Rare:75 | ||||
| chr11:9460717-9461014 | Common:3; Rare:84 | ||||
| chr11:10304917-10305077 | Common:1; Rare:31 | ||||
| chr11:10541167-10541262 | Rare:30 | ||||
| chr11:10693504-10693659 | Common:1; Rare:52 | ||||
| chr11:10751141-10751300 | Rare:49 | ||||
| chr11:10800205-10800731 | Common:1; Rare:154 | ||||
| chr11:10858030-10858252 | Common:2; Rare:68 | ||||
| chr11:16738773-16738836 | Rare:17 | ||||
| chr11:17310922-17311240 | Rare:67 | ||||
| chr11:18322116-18322279 | Common:3; Rare:58; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:18322457-18322582 | Common:2; Rare:50 | ||||
| chr11:18526877-18526968 | Rare:42 | ||||
| chr11:18588661-18588870 | Common:2; Rare:73 |