| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:14520297-14520495 | Rare:67 | ||||
| chr11:14892190-14892369 | Rare:55 | ||||
| chr11:16738436-16738854 | Common:3; Rare:102 | ||||
| chr11:17077608-17077877 | Common:2; Rare:113 | ||||
| chr11:17207870-17208111 | Common:2; Rare:87 | ||||
| chr11:17276579-17276828 | Common:3; Rare:64; Clinvar:3 | ||||
| chr11:18322119-18322347 | Common:6; Rare:89; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:18322437-18322645 | Common:2; Rare:80 | ||||
| chr11:18394401-18394633 | Common:1; Rare:92; Clinvar (benign):1 | ||||
| chr11:18526841-18526993 | Rare:74 | ||||
| chr11:18588667-18588929 | Common:3; Rare:86 | ||||
| chr11:18634332-18634566 | Common:2; Rare:74 | ||||
| chr11:18698496-18698830 | Common:6; Rare:83 | ||||
| chr11:20363659-20363788 | Common:3; Rare:28 | ||||
| chr11:22625518-22625609 | Rare:46; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 |