| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:10857211-10857341 | Rare:26 | ||||
| chr11:10857370-10857633 | Common:1; Rare:54 | ||||
| chr11:10858023-10858286 | Common:2; Rare:83 | ||||
| chr11:14520303-14520443 | Rare:46 | ||||
| chr11:16738453-16738750 | Common:3; Rare:67 | ||||
| chr11:16738761-16738836 | Rare:18 | ||||
| chr11:17077628-17077868 | Common:2; Rare:99 | ||||
| chr11:17207950-17208093 | Common:1; Rare:53 | ||||
| chr11:18013010-18013237 | Common:5; Rare:71 | ||||
| chr11:18322111-18322314 | Common:3; Rare:76; Clinvar:2; Clinvar (benign):2 | ||||
| chr11:18322474-18322586 | Common:2; Rare:47 | ||||
| chr11:18526863-18526980 | Rare:56 | ||||
| chr11:18588667-18588795 | Rare:47 | ||||
| chr11:18634332-18634580 | Common:2; Rare:79 | ||||
| chr11:20363657-20363788 | Common:3; Rare:28 |