| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:28348614-28348724 | Rare:27 | ||||
| chr3:28348779-28349179 | Common:3; Rare:128 | ||||
| chr3:29280806-29281103 | Common:3; Rare:62 | ||||
| chr3:30606341-30606592 | Common:1; Rare:68; Clinvar:3; Clinvar (benign):1 | ||||
| chr3:31532292-31532654 | Common:5; Rare:113 | ||||
| chr3:31532815-31533204 | Common:2; Rare:159; Clinvar (benign):2 | ||||
| chr3:31960170-31960385 | Common:2; Rare:37 | ||||
| chr3:31981018-31981080 | Common:1; Rare:23 | ||||
| chr3:31981250-31981454 | Common:1; Rare:44 | ||||
| chr3:31981613-31981846 | Common:1; Rare:59 | ||||
| chr3:32238560-32238753 | Common:2; Rare:54 | ||||
| chr3:32391653-32391988 | Common:5; Rare:92 | ||||
| chr3:32502679-32503093 | Rare:106 | ||||
| chr3:32570747-32570900 | Rare:70 | ||||
| chr3:32685118-32685460 | Rare:92 |