| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:66473332-66473424 | Rare:19 | ||||
| chr3:66473656-66473958 | Common:2; Rare:62 | ||||
| chr3:66499338-66499498 | Common:1; Rare:35 | ||||
| chr3:66499828-66499916 | Common:2; Rare:14 | ||||
| chr3:66500178-66500318 | Common:1; Rare:43 | ||||
| chr3:66798940-66799018 | Common:1; Rare:9 | ||||
| chr3:67429923-67430045 | Common:1; Rare:27 | ||||
| chr3:67513763-67514030 | Common:4; Rare:74 | ||||
| chr3:67592418-67592722 | Common:3; Rare:45 | ||||
| chr3:68981725-68981893 | Common:4; Rare:31 | ||||
| chr3:68985738-68985824 | Rare:19 | ||||
| chr3:68991112-68991212 | Rare:11 | ||||
| chr3:69007816-69007982 | Rare:38 | ||||
| chr3:69008233-69008482 | Rare:62; Clinvar (pathogenic):1 | ||||
| chr3:69008914-69009240 | Common:1; Rare:49 |