| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:14520283-14520526 | Rare:85 | ||||
| chr11:14891589-14891803 | Rare:64 | ||||
| chr11:16738450-16738854 | Common:3; Rare:97 | ||||
| chr11:17077607-17077847 | Common:2; Rare:99 | ||||
| chr11:17207898-17208098 | Common:2; Rare:78 | ||||
| chr11:17276508-17276822 | Common:5; Rare:92; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr11:18322108-18322345 | Common:6; Rare:93; Clinvar:2; Clinvar (benign):2 | ||||
| chr11:18322467-18322626 | Common:2; Rare:67 | ||||
| chr11:18526841-18526977 | Rare:66 | ||||
| chr11:18588667-18588899 | Common:2; Rare:80 | ||||
| chr11:18634283-18634592 | Common:3; Rare:108 | ||||
| chr11:18698470-18698845 | Common:6; Rare:93 | ||||
| chr11:20364117-20364181 | Rare:16 | ||||
| chr11:20387417-20387758 | Common:7; Rare:113 | ||||
| chr11:22625808-22625960 | Common:2; Rare:56; Clinvar:2; Clinvar (benign):1 |