| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:92145402-92145655 | Common:2; Rare:105 | ||||
| chr12:92145802-92146215 | Common:4; Rare:139 | ||||
| chr12:92929102-92929513 | Common:2; Rare:124 | ||||
| chr12:93377728-93377956 | Rare:74 | ||||
| chr12:93378190-93378419 | Common:1; Rare:54 | ||||
| chr12:93441856-93442173 | Common:2; Rare:100 | ||||
| chr12:93569683-93570029 | Common:2; Rare:64 | ||||
| chr12:93570254-93570389 | Common:1; Rare:25 | ||||
| chr12:93570827-93571305 | Common:1; Rare:112 | ||||
| chr12:93571731-93571912 | Common:7; Rare:69 | ||||
| chr12:93677321-93677453 | Rare:29 | ||||
| chr12:94459802-94460064 | Common:3; Rare:76 | ||||
| chr12:94650446-94650787 | Common:2; Rare:88 | ||||
| chr12:95003593-95003830 | Common:3; Rare:99; Clinvar (benign):6 | ||||
| chr12:95073439-95073663 | Common:1; Rare:79 |