| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:123194828-123195086 | Common:3; Rare:85 | ||||
| chr11:123195090-123195235 | Rare:29 | ||||
| chr11:123195289-123195402 | Common:2; Rare:18 | ||||
| chr11:123195715-123195823 | Common:1; Rare:22 | ||||
| chr11:123654559-123654775 | Common:5; Rare:58; Clinvar (benign):1 | ||||
| chr11:123741249-123741448 | Rare:44 | ||||
| chr11:123741528-123741831 | Common:2; Rare:75 | ||||
| chr11:124622700-124623010 | Common:5; Rare:101 | ||||
| chr11:124623099-124623256 | Rare:48 | ||||
| chr11:124673425-124673501 | Rare:16 | ||||
| chr11:124673641-124674059 | Common:5; Rare:116 | ||||
| chr11:124739776-124739991 | Rare:68 | ||||
| chr11:124762234-124762495 | Rare:66 | ||||
| chr11:124762770-124762922 | Common:1; Rare:38 | ||||
| chr11:124800325-124800513 | Common:1; Rare:74 |