| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:130053785-130053939 | Common:1; Rare:46 | ||||
| chr9:130053858-130053963 | Common:1; Rare:43 | ||||
| chr9:130579424-130579703 | Common:14; Rare:209 | ||||
| chr9:130693533-130693815 | Common:1; Rare:160 | ||||
| chr9:130835116-130835389 | Common:16; Rare:149 | ||||
| chr9:131125372-131125717 | Common:5; Rare:297 | ||||
| chr9:131393736-131394203 | Common:2; Rare:321 | ||||
| chr9:131502832-131503052 | Rare:150; Clinvar:6 | ||||
| chr9:131531156-131531397 | Common:19; Rare:193 | ||||
| chr9:132354854-132355293 | Common:9; Rare:262 | ||||
| chr9:132669480-132669750 | Rare:105 | ||||
| chr9:132669927-132670086 | Common:2; Rare:135 | ||||
| chr9:132670392-132670574 | Rare:123 | ||||
| chr9:132878130-132878420 | Common:3; Rare:150 | ||||
| chr9:132944560-132945090 | Common:1; Rare:291; Clinvar:2; Clinvar (benign):1 |