| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:123741607-123741799 | Common:2; Rare:58 | ||||
| chr11:124673853-124673929 | Common:3; Rare:16 | ||||
| chr11:124762277-124762405 | Rare:33 | ||||
| chr11:124800406-124800471 | Rare:23 | ||||
| chr11:125164494-125164759 | Rare:50 | ||||
| chr11:125495428-125495611 | Common:4; Rare:65 | ||||
| chr11:125496101-125496466 | Common:2; Rare:75 | ||||
| chr11:125592478-125592909 | Common:6; Rare:143 | ||||
| chr11:125625850-125625959 | Rare:40 | ||||
| chr11:125887360-125887647 | Common:2; Rare:80 | ||||
| chr11:125887651-125887737 | Common:1; Rare:35 | ||||
| chr11:125903188-125903249 | Rare:15 | ||||
| chr11:125904249-125904520 | Common:1; Rare:85 | ||||
| chr11:126211624-126211812 | Rare:87 | ||||
| chr11:126268835-126269214 | Common:2; Rare:143; Clinvar:3; Clinvar (benign):4 |