| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:123063303-123063449 | Rare:34 | ||||
| chr11:123194480-123194800 | Common:2; Rare:60 | ||||
| chr11:123194868-123194973 | Common:1; Rare:41 | ||||
| chr11:123454255-123454443 | Common:2; Rare:25 | ||||
| chr11:123654559-123654719 | Common:3; Rare:42; Clinvar (benign):1 | ||||
| chr11:123741529-123741799 | Common:2; Rare:67 | ||||
| chr11:124115296-124115483 | Common:2; Rare:33 | ||||
| chr11:124622561-124622916 | Common:7; Rare:103 | ||||
| chr11:124673659-124673974 | Common:5; Rare:94 | ||||
| chr11:124674090-124674213 | Rare:29 | ||||
| chr11:124739823-124739969 | Rare:39 | ||||
| chr11:124762268-124762455 | Rare:46 | ||||
| chr11:124800345-124800746 | Common:2; Rare:123 | ||||
| chr11:124876047-124876190 | Rare:56 | ||||
| chr11:124876375-124876482 | Rare:35; Clinvar:2; Clinvar (benign):1 |