| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:14520290-14520479 | Rare:60 | ||||
| chr11:16738466-16738725 | Common:3; Rare:56 | ||||
| chr11:17207910-17208111 | Common:2; Rare:76 | ||||
| chr11:17276463-17276813 | Common:4; Rare:100; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr11:18106037-18106308 | Common:2; Rare:83 | ||||
| chr11:18322131-18322332 | Common:5; Rare:75; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:18322457-18322638 | Common:2; Rare:75 | ||||
| chr11:18526809-18527014 | Common:1; Rare:98 | ||||
| chr11:18588667-18588838 | Common:2; Rare:56 | ||||
| chr11:18634332-18634588 | Common:2; Rare:82 | ||||
| chr11:18634794-18634874 | Rare:12 | ||||
| chr11:20363659-20363781 | Common:2; Rare:26 | ||||
| chr11:20387410-20387786 | Common:8; Rare:120 | ||||
| chr11:22625808-22626002 | Common:2; Rare:68; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:22829333-22829414 | Common:1; Rare:21 |