| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:133348039-133348260 | Common:2; Rare:88 | ||||
| chr9:133356443-133356616 | Common:1; Rare:81; Clinvar (benign):2 | ||||
| chr9:133375965-133376368 | Common:3; Rare:146 | ||||
| chr9:134135263-134135414 | Common:2; Rare:30 | ||||
| chr9:134641556-134641809 | Common:2; Rare:79; Clinvar (benign):1 | ||||
| chr9:135499855-135499966 | Common:3; Rare:31 | ||||
| chr9:136410583-136410678 | Common:1; Rare:52 | ||||
| chr9:136411124-136411233 | Common:1; Rare:25 | ||||
| chr9:136745881-136746220 | Common:1; Rare:91 | ||||
| chr9:136886240-136886531 | Common:2; Rare:87 | ||||
| chr9:136943497-136943719 | Common:2; Rare:89 | ||||
| chr9:136944592-136944924 | Common:2; Rare:129 | ||||
| chr9:136977360-136977826 | Common:2; Rare:116 | ||||
| chr9:136977900-136978151 | Rare:58 | ||||
| chr9:136979927-136980274 | Rare:136 |