| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:125063163-125063305 | Common:2; Rare:41 | ||||
| chr11:125111710-125111984 | Common:3; Rare:55 | ||||
| chr11:125164533-125164769 | Rare:43 | ||||
| chr11:125569245-125569572 | Common:2; Rare:96 | ||||
| chr11:125592456-125592932 | Common:6; Rare:161 | ||||
| chr11:125625844-125625980 | Common:1; Rare:47 | ||||
| chr11:125903179-125903355 | Rare:44 | ||||
| chr11:125904299-125904515 | Rare:71 | ||||
| chr11:126062627-126063029 | Common:7; Rare:131 | ||||
| chr11:126211620-126211819 | Rare:91 | ||||
| chr11:126266188-126266419 | Rare:80 | ||||
| chr11:126268338-126268613 | Common:3; Rare:60 | ||||
| chr11:126268761-126269209 | Common:2; Rare:175; Clinvar:2; Clinvar (benign):4 | ||||
| chr11:126282959-126283131 | Common:1; Rare:59 | ||||
| chr11:126303952-126304090 | Rare:81 |