| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:131125407-131125657 | Common:2; Rare:117 | ||||
| chr9:131531182-131531336 | Common:9; Rare:69 | ||||
| chr9:132354922-132355295 | Common:5; Rare:122 | ||||
| chr9:132669939-132670040 | Common:1; Rare:49 | ||||
| chr9:132670277-132670503 | Rare:63 | ||||
| chr9:132878262-132878381 | Common:1; Rare:45 | ||||
| chr9:133030465-133030753 | Common:4; Rare:79 | ||||
| chr9:133336110-133336345 | Common:1; Rare:101 | ||||
| chr9:133348030-133348313 | Common:4; Rare:122 | ||||
| chr9:133356476-133356628 | Common:1; Rare:71; Clinvar (benign):2 | ||||
| chr9:133375999-133376340 | Common:1; Rare:125 | ||||
| chr9:133479057-133479334 | Common:1; Rare:88 | ||||
| chr9:136410317-136410706 | Common:7; Rare:166 | ||||
| chr9:136659249-136659470 | Common:2; Rare:52 | ||||
| chr9:136662697-136663024 | Common:2; Rare:74 |