| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:37903676-37903813 | Rare:32 | ||||
| chr9:37904059-37904432 | Common:3; Rare:125 | ||||
| chr9:38620543-38620778 | Rare:66 | ||||
| chr9:43127097-43127376 | Common:2; Rare:79 | ||||
| chr9:65675693-65675989 | Common:1; Rare:79 | ||||
| chr9:68356388-68356629 | Common:7; Rare:42 | ||||
| chr9:68356746-68357134 | Common:5; Rare:99 | ||||
| chr9:68739882-68740146 | Common:1; Rare:43 | ||||
| chr9:68779798-68780162 | Common:6; Rare:121 | ||||
| chr9:68780280-68780334 | Rare:20 | ||||
| chr9:69035558-69035795 | Common:2; Rare:47; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr9:69120850-69121517 | Common:3; Rare:147 | ||||
| chr9:69759921-69760113 | Common:2; Rare:88 | ||||
| chr9:70043789-70043962 | Rare:34 | ||||
| chr9:70044026-70044178 | Rare:29 |