| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:106139447-106139600 | Common:2; Rare:42 | ||||
| chr12:106247356-106247818 | Common:6; Rare:150 | ||||
| chr12:106247822-106248377 | Common:2; Rare:148 | ||||
| chr12:106301783-106301815 | Rare:5 | ||||
| chr12:106301838-106302088 | Common:2; Rare:48 | ||||
| chr12:106302179-106302299 | Rare:30 | ||||
| chr12:106302438-106302678 | Common:2; Rare:56 | ||||
| chr12:106302716-106303007 | Common:7; Rare:69 | ||||
| chr12:106303148-106303568 | Common:1; Rare:105 | ||||
| chr12:106357677-106357850 | Common:3; Rare:47; Clinvar:4; Clinvar (benign):1 | ||||
| chr12:106357909-106358202 | Common:4; Rare:122 | ||||
| chr12:106358252-106358362 | Rare:27 | ||||
| chr12:106358364-106358689 | Common:2; Rare:63 | ||||
| chr12:106773973-106774435 | Common:3; Rare:113 | ||||
| chr12:106774465-106774779 | Common:2; Rare:94 |