| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:51324037-51324291 | Rare:76 | ||||
| chr12:51391354-51391472 | Common:1; Rare:28 | ||||
| chr12:51391592-51391737 | Common:1; Rare:43 | ||||
| chr12:51424660-51424870 | Common:1; Rare:52 | ||||
| chr12:51911884-51912108 | Common:3; Rare:21 | ||||
| chr12:51912210-51912525 | Common:2; Rare:79; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:52006811-52006946 | Rare:20 | ||||
| chr12:52013578-52013621 | Rare:4 | ||||
| chr12:52051152-52051523 | Common:1; Rare:123 | ||||
| chr12:52055858-52056072 | Common:3; Rare:67 | ||||
| chr12:52069641-52070232 | Common:2; Rare:180 | ||||
| chr12:52232735-52232760 | Rare:7 | ||||
| chr12:52233060-52233646 | Common:5; Rare:194 | ||||
| chr12:52813880-52814283 | Common:1; Rare:134; Clinvar:3; Clinvar (benign):2 | ||||
| chr12:52904642-52905353 | Common:7; Rare:201; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):2 |