| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:133347962-133348313 | Common:4; Rare:130 | ||||
| chr9:133356399-133356648 | Common:1; Rare:120; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr9:133375965-133376366 | Common:3; Rare:146 | ||||
| chr9:133417901-133418116 | Common:3; Rare:59 | ||||
| chr9:133479066-133479230 | Rare:52 | ||||
| chr9:134135263-134135430 | Common:2; Rare:31 | ||||
| chr9:135501225-135501422 | Common:2; Rare:56 | ||||
| chr9:135502319-135502497 | Common:1; Rare:35 | ||||
| chr9:135521073-135521515 | Common:4; Rare:91 | ||||
| chr9:135961125-135961534 | Common:6; Rare:150 | ||||
| chr9:136118812-136119041 | Common:4; Rare:98 | ||||
| chr9:136410372-136410686 | Common:6; Rare:136 | ||||
| chr9:136687365-136687658 | Common:2; Rare:83; Clinvar:4; Clinvar (benign):1 | ||||
| chr9:136807797-136808115 | Common:2; Rare:120 | ||||
| chr9:136848659-136848816 | Common:1; Rare:45 |