| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:123560186-123560340 | Rare:28 | ||||
| chr11:123654552-123654727 | Common:3; Rare:44; Clinvar (benign):1 | ||||
| chr11:124673724-124673929 | Common:4; Rare:60 | ||||
| chr11:124739782-124739947 | Rare:49 | ||||
| chr11:124800397-124800471 | Rare:27 | ||||
| chr11:124953983-124954149 | Common:3; Rare:46 | ||||
| chr11:125495414-125495569 | Common:4; Rare:56 | ||||
| chr11:125496121-125496466 | Rare:73 | ||||
| chr11:125569234-125569545 | Common:2; Rare:92 | ||||
| chr11:125592506-125592917 | Common:6; Rare:132 | ||||
| chr11:125625869-125625952 | Rare:30 | ||||
| chr11:125887480-125887727 | Common:2; Rare:78 | ||||
| chr11:125903188-125903271 | Rare:20 | ||||
| chr11:125904203-125904520 | Common:1; Rare:94 | ||||
| chr11:126211641-126211809 | Rare:77 |