| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:129642077-129642198 | Common:1; Rare:36 | ||||
| chr9:129752955-129753148 | Common:2; Rare:61 | ||||
| chr9:129803084-129803225 | Rare:59 | ||||
| chr9:129803405-129803521 | Common:1; Rare:38 | ||||
| chr9:129824081-129824265 | Common:2; Rare:52; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:129834710-129834960 | Common:4; Rare:76 | ||||
| chr9:129835112-129835524 | Common:4; Rare:161 | ||||
| chr9:130043053-130043290 | Common:2; Rare:74 | ||||
| chr9:130053587-130053741 | Rare:33 | ||||
| chr9:130053804-130054071 | Common:1; Rare:89 | ||||
| chr9:130579427-130579878 | Common:7; Rare:159 | ||||
| chr9:130693637-130693800 | Rare:56 | ||||
| chr9:130713411-130713657 | Common:2; Rare:54 | ||||
| chr9:130835165-130835373 | Common:8; Rare:64 | ||||
| chr9:131096321-131096599 | Common:3; Rare:74 |