| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:155854355-155854765 | Rare:111 | ||||
| chr3:155870323-155870714 | Common:2; Rare:114 | ||||
| chr3:156674362-156674706 | Common:3; Rare:99 | ||||
| chr3:156826187-156826311 | Common:1; Rare:39 | ||||
| chr3:157160033-157160295 | Rare:107 | ||||
| chr3:158105732-158105861 | Common:5; Rare:69; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:158672549-158672700 | Common:2; Rare:40 | ||||
| chr3:158732141-158732356 | Common:7; Rare:59 | ||||
| chr3:158732777-158732848 | Rare:11 | ||||
| chr3:158801984-158802178 | Common:2; Rare:90 | ||||
| chr3:159763165-159763347 | Rare:32 | ||||
| chr3:159763569-159763727 | Rare:45 | ||||
| chr3:159764331-159764550 | Common:1; Rare:59 | ||||
| chr3:159852936-159853342 | Rare:75 | ||||
| chr3:160399167-160399353 | Rare:52; Clinvar:3 |