| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:110742830-110743256 | Common:3; Rare:142 | ||||
| chr12:111368977-111369283 | Common:1; Rare:80 | ||||
| chr12:111405273-111405477 | Common:1; Rare:36 | ||||
| chr12:111405745-111405990 | Rare:78 | ||||
| chr12:111597409-111597551 | Rare:24 | ||||
| chr12:111597915-111598013 | Rare:27 | ||||
| chr12:111598892-111599135 | Common:14; Rare:154; Clinvar (benign):5 | ||||
| chr12:111599193-111599696 | Common:4; Rare:172; Clinvar (benign):1 | ||||
| chr12:111599721-111599918 | Rare:46 | ||||
| chr12:111599985-111600078 | Rare:25 | ||||
| chr12:111685472-111685594 | Common:1; Rare:27 | ||||
| chr12:111685741-111686184 | Rare:157 | ||||
| chr12:111686266-111686425 | Common:1; Rare:33 | ||||
| chr12:111686434-111686670 | Rare:55 | ||||
| chr12:111766367-111766539 | Common:2; Rare:31 |