| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:14520314-14520464 | Rare:43 | ||||
| chr11:16738456-16738823 | Common:3; Rare:82 | ||||
| chr11:17207905-17208102 | Common:2; Rare:77 | ||||
| chr11:17276463-17276812 | Common:4; Rare:100; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr11:18322113-18322332 | Common:5; Rare:86; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:18322457-18322631 | Common:2; Rare:72 | ||||
| chr11:18526813-18526987 | Rare:81 | ||||
| chr11:18588672-18588809 | Rare:48 | ||||
| chr11:18634330-18634588 | Common:2; Rare:82 | ||||
| chr11:20363683-20363788 | Common:2; Rare:24 | ||||
| chr11:22624861-22625165 | Common:2; Rare:112; Clinvar:7; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr11:22625507-22625604 | Rare:48; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr11:22625808-22626002 | Common:2; Rare:68; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:27506738-27506868 | Common:1; Rare:56 | ||||
| chr11:28108127-28108414 | Common:1; Rare:85 |