| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:131125366-131125649 | Common:3; Rare:130 | ||||
| chr9:133030445-133030759 | Common:4; Rare:90 | ||||
| chr9:133348039-133348268 | Common:2; Rare:93 | ||||
| chr9:133356372-133356592 | Common:3; Rare:92; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr9:133375995-133376366 | Common:2; Rare:134 | ||||
| chr9:133417963-133418082 | Common:1; Rare:30 | ||||
| chr9:134917808-134918027 | Common:2; Rare:65 | ||||
| chr9:136118871-136119044 | Common:1; Rare:76 | ||||
| chr9:136373585-136373780 | Rare:42; Clinvar:4 | ||||
| chr9:136410396-136410671 | Common:6; Rare:117 | ||||
| chr9:136807780-136808106 | Common:2; Rare:130 | ||||
| chr9:137032404-137032579 | Common:1; Rare:37 | ||||
| chr9:137033026-137033216 | Common:2; Rare:71 | ||||
| chr9:137087033-137087110 | Rare:33; Clinvar:1 | ||||
| chr9:137113115-137113214 | Rare:50 |