| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:8681404-8681671 | Common:4; Rare:51 | ||||
| chr12:8823032-8823242 | Rare:58; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:8949392-8949555 | Rare:23 | ||||
| chr12:8949563-8950097 | Common:4; Rare:126 | ||||
| chr12:9869317-9869649 | Common:3; Rare:51 | ||||
| chr12:10213403-10213637 | Common:1; Rare:55 | ||||
| chr12:10613532-10613663 | Common:1; Rare:55 | ||||
| chr12:10673978-10674145 | Common:1; Rare:34 | ||||
| chr12:10715757-10715812 | Rare:19 | ||||
| chr12:10718328-10718451 | Rare:23 | ||||
| chr12:10718668-10718939 | Rare:51 | ||||
| chr12:10723285-10723468 | Common:5; Rare:56 | ||||
| chr12:11170948-11171303 | Common:5; Rare:97 | ||||
| chr12:11171429-11171458 | Rare:5 | ||||
| chr12:11171527-11171733 | Common:2; Rare:65 |