| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:131502765-131502863 | Rare:38 | ||||
| chr3:131502865-131503023 | Common:1; Rare:64 | ||||
| chr3:132037702-132037897 | Common:1; Rare:31 | ||||
| chr3:132417165-132417713 | Common:6; Rare:179 | ||||
| chr3:132659799-132659965 | Common:3; Rare:38 | ||||
| chr3:133038131-133038419 | Common:1; Rare:100 | ||||
| chr3:133124561-133124913 | Common:1; Rare:73 | ||||
| chr3:133573815-133574030 | Rare:74 | ||||
| chr3:133661758-133662033 | Rare:61 | ||||
| chr3:133895218-133895589 | Rare:101 | ||||
| chr3:134485386-134485772 | Rare:91 | ||||
| chr3:134485957-134486222 | Common:2; Rare:91 | ||||
| chr3:135965484-135965844 | Common:1; Rare:141 | ||||
| chr3:136196562-136196653 | Rare:24 | ||||
| chr3:136250232-136250426 | Common:3; Rare:84; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):2 |