| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:123061572-123061669 | Common:2; Rare:36 | ||||
| chr11:123062879-123063208 | Common:3; Rare:119 | ||||
| chr11:123063398-123063522 | Rare:26 | ||||
| chr11:123063649-123063748 | Common:1; Rare:17 | ||||
| chr11:123083723-123083841 | Common:1; Rare:30; Clinvar (pathogenic):1 | ||||
| chr11:123194692-123194821 | Common:2; Rare:19 | ||||
| chr11:123194832-123195075 | Common:3; Rare:78 | ||||
| chr11:123195222-123195451 | Common:2; Rare:38 | ||||
| chr11:123195471-123195566 | Rare:17 | ||||
| chr11:123654562-123654797 | Common:5; Rare:63; Clinvar (benign):1 | ||||
| chr11:123741243-123741297 | Rare:12 | ||||
| chr11:123741300-123741385 | Rare:14 | ||||
| chr11:123741519-123741831 | Common:2; Rare:78 | ||||
| chr11:124115293-124115515 | Common:2; Rare:43 | ||||
| chr11:124622435-124622499 | Common:1; Rare:12 |