| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:8033167-8033318 | Common:2; Rare:38 | ||||
| chr12:8033481-8033823 | Common:2; Rare:80 | ||||
| chr12:8227606-8227691 | Rare:24 | ||||
| chr12:8697728-8698086 | Common:2; Rare:133 | ||||
| chr12:8822469-8822712 | Rare:59; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr12:8949960-8950057 | Common:1; Rare:24 | ||||
| chr12:10613533-10613725 | Common:1; Rare:78 | ||||
| chr12:10715596-10715822 | Rare:72 | ||||
| chr12:10722301-10722398 | Rare:25 | ||||
| chr12:10722752-10723022 | Common:3; Rare:85 | ||||
| chr12:10723134-10723459 | Common:5; Rare:103 | ||||
| chr12:11171158-11171261 | Common:2; Rare:42 | ||||
| chr12:11171559-11171725 | Common:2; Rare:57 | ||||
| chr12:12357020-12357220 | Common:4; Rare:99 | ||||
| chr12:12560898-12561199 | Common:4; Rare:63 |