| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6899969-6900260 | Common:5; Rare:50 | ||||
| chr12:6925401-6925999 | Common:2; Rare:194 | ||||
| chr12:6925983-6926247 | Common:4; Rare:69 | ||||
| chr12:6927289-6927569 | Rare:51 | ||||
| chr12:6961297-6961542 | Common:2; Rare:52 | ||||
| chr12:6961777-6962247 | Common:8; Rare:195 | ||||
| chr12:6962329-6962850 | Common:12; Rare:249 | ||||
| chr12:6962984-6963337 | Common:4; Rare:180 | ||||
| chr12:6963364-6963764 | Common:6; Rare:200 | ||||
| chr12:6963997-6964397 | Common:3; Rare:127 | ||||
| chr12:6965730-6966197 | Common:4; Rare:204 | ||||
| chr12:6974051-6974528 | Common:1; Rare:214; Clinvar (pathogenic):1 | ||||
| chr12:6998751-6999576 | Common:2; Rare:180 | ||||
| chr12:7439630-7440744 | Common:19; Rare:644 | ||||
| chr12:7555875-7556061 | Common:1; Rare:36 |