| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:4320670-4320740 | Common:1; Rare:15 | ||||
| chr12:4320844-4321275 | Common:6; Rare:160 | ||||
| chr12:4538388-4538976 | Common:3; Rare:151 | ||||
| chr12:4539095-4539190 | Rare:18 | ||||
| chr12:4604892-4605013 | Rare:52 | ||||
| chr12:4648960-4649233 | Common:2; Rare:87; Clinvar (benign):2 | ||||
| chr12:4649346-4649408 | Rare:8 | ||||
| chr12:6200229-6200374 | Common:2; Rare:36 | ||||
| chr12:6341418-6341503 | Common:1; Rare:21 | ||||
| chr12:6342073-6342198 | Common:1; Rare:26 | ||||
| chr12:6363327-6363477 | Common:2; Rare:59; Clinvar (benign):1 | ||||
| chr12:6383968-6384221 | Common:1; Rare:64 | ||||
| chr12:6451244-6451277 | Rare:8 | ||||
| chr12:6451433-6451703 | Common:1; Rare:64 | ||||
| chr12:6451753-6451863 | Rare:17 |