| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:31117044-31117334 | Common:5; Rare:129 | ||||
| chr12:31324080-31324478 | Common:2; Rare:89 | ||||
| chr12:31326027-31326514 | Common:4; Rare:148 | ||||
| chr12:31591159-31591292 | Rare:45 | ||||
| chr12:31659115-31659229 | Common:1; Rare:39 | ||||
| chr12:31728995-31729386 | Common:1; Rare:119 | ||||
| chr12:31959245-31959482 | Common:2; Rare:77 | ||||
| chr12:32501984-32502274 | Common:2; Rare:62; Clinvar:3; Clinvar (benign):2 | ||||
| chr12:32679050-32679358 | Common:2; Rare:122; Clinvar:1; Clinvar (benign):4 | ||||
| chr12:32755231-32755371 | Common:1; Rare:45; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr12:32755861-32756030 | Common:1; Rare:61 | ||||
| chr12:32896764-32896981 | Common:1; Rare:72; Clinvar:4; Clinvar (benign):2 | ||||
| chr12:34022337-34022582 | Common:3; Rare:68 | ||||
| chr12:38905526-38905684 | Common:3; Rare:46 | ||||
| chr12:38905692-38905820 | Common:3; Rare:40 |