| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:131107988-131108196 | Common:1; Rare:29 | ||||
| chr8:8244580-8244795 | Common:2; Rare:77 | ||||
| chr8:22950607-22950803 | Common:1; Rare:41 | ||||
| chr8:30423287-30423424 | Common:1; Rare:28 | ||||
| chr8:30541811-30542062 | Common:1; Rare:43 | ||||
| chr8:47737398-47737773 | Common:2; Rare:116 | ||||
| chr8:107497259-107497393 | Common:1; Rare:35 | ||||
| chr8:145002827-145003035 | Common:2; Rare:71 | ||||
| chr9:39810022-39810286 | Common:2; Rare:8 | ||||
| chr9:40991953-40992390 | Common:7; Rare:32 | ||||
| chr9:70413429-70413670 | Rare:79 | ||||
| chr9:70413950-70414068 | Rare:20 | ||||
| chr9:83219218-83219357 | Common:2; Rare:36 | ||||
| chr9:124356422-124356695 | Common:1; Rare:42 | ||||
| chr9:128617809-128617987 | Common:2; Rare:40; Clinvar (benign):1 |