| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:124622678-124623005 | Common:5; Rare:101 | ||||
| chr11:124623125-124623249 | Rare:34 | ||||
| chr11:124623269-124623394 | Common:2; Rare:30 | ||||
| chr11:124673682-124674044 | Common:5; Rare:104 | ||||
| chr11:124674080-124674251 | Rare:38 | ||||
| chr11:124739780-124739983 | Rare:65 | ||||
| chr11:124740339-124740399 | Rare:7 | ||||
| chr11:124800029-124800146 | Common:1; Rare:37 | ||||
| chr11:124800298-124800908 | Common:3; Rare:167 | ||||
| chr11:124876101-124876190 | Rare:39 | ||||
| chr11:124876323-124876577 | Common:1; Rare:85; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:124876619-124876892 | Common:3; Rare:56 | ||||
| chr11:124953842-124954249 | Common:5; Rare:104 | ||||
| chr11:124954313-124954412 | Rare:24 | ||||
| chr11:125062967-125063110 | Common:1; Rare:30 |