| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:124673818-124673940 | Common:4; Rare:24 | ||||
| chr11:124762219-124762428 | Rare:55 | ||||
| chr11:124800406-124800466 | Rare:20 | ||||
| chr11:124935993-124936073 | Common:1; Rare:20; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:124953962-124954202 | Common:5; Rare:72 | ||||
| chr11:125111712-125112010 | Common:3; Rare:62 | ||||
| chr11:125164516-125164759 | Rare:45 | ||||
| chr11:125495414-125495569 | Common:4; Rare:56 | ||||
| chr11:125496130-125496437 | Rare:69 | ||||
| chr11:125569242-125569545 | Common:2; Rare:91 | ||||
| chr11:125592478-125592930 | Common:6; Rare:151 | ||||
| chr11:125625850-125626008 | Rare:52 | ||||
| chr11:125887480-125887727 | Common:2; Rare:78 | ||||
| chr11:125903183-125903355 | Rare:43 | ||||
| chr11:126211641-126211809 | Rare:77 |