| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:133336130-133336386 | Common:2; Rare:219 | ||||
| chr9:133347768-133348303 | Common:12; Rare:322 | ||||
| chr9:133356446-133356657 | Common:2; Rare:167; Clinvar (benign):4 | ||||
| chr9:133375354-133375530 | Rare:49 | ||||
| chr9:133375933-133376381 | Common:7; Rare:297 | ||||
| chr9:133417876-133418324 | Common:6; Rare:158 | ||||
| chr9:133459740-133460250 | Common:4; Rare:263 | ||||
| chr9:133479055-133479230 | Rare:59 | ||||
| chr9:133479420-133479830 | Common:4; Rare:121 | ||||
| chr9:133992258-133992486 | Rare:140 | ||||
| chr9:133992702-133992967 | Common:1; Rare:164 | ||||
| chr9:134067917-134068251 | Rare:169 | ||||
| chr9:134068360-134068730 | Common:10; Rare:248 | ||||
| chr9:134135282-134135476 | Common:3; Rare:43 | ||||
| chr9:134135470-134135670 | Common:2; Rare:88 |