| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:129140055-129140145 | Rare:22 | ||||
| chr9:129141497-129141688 | Common:3; Rare:57 | ||||
| chr9:129626109-129626231 | Rare:45 | ||||
| chr9:129803074-129803235 | Common:2; Rare:64 | ||||
| chr9:129824081-129824303 | Common:3; Rare:61; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:129835210-129835517 | Common:3; Rare:122 | ||||
| chr9:130042978-130043361 | Common:3; Rare:121 | ||||
| chr9:130043641-130043879 | Common:2; Rare:48 | ||||
| chr9:130053635-130053741 | Rare:21 | ||||
| chr9:130053743-130054071 | Common:1; Rare:101 | ||||
| chr9:130200200-130200427 | Common:3; Rare:33 | ||||
| chr9:130579410-130579878 | Common:7; Rare:167 | ||||
| chr9:130834887-130835026 | Common:1; Rare:41 | ||||
| chr9:130835095-130835485 | Common:11; Rare:122 | ||||
| chr9:131125435-131125667 | Common:1; Rare:112 |