| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:49130785-49130906 | Common:3; Rare:49 | ||||
| chr12:49131341-49131626 | Common:2; Rare:110 | ||||
| chr12:49188468-49188607 | Common:2; Rare:18 | ||||
| chr12:49188981-49189346 | Rare:95; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:49227491-49228024 | Common:1; Rare:93 | ||||
| chr12:49264781-49265085 | Common:4; Rare:108 | ||||
| chr12:49322986-49323324 | Common:3; Rare:76 | ||||
| chr12:49367202-49367530 | Common:1; Rare:90 | ||||
| chr12:49568089-49568389 | Common:2; Rare:74 | ||||
| chr12:49623319-49623571 | Common:1; Rare:65 | ||||
| chr12:49828374-49828579 | Common:1; Rare:78 | ||||
| chr12:49903856-49904179 | Common:3; Rare:82 | ||||
| chr12:50025407-50025717 | Common:2; Rare:85 | ||||
| chr12:50085055-50085364 | Common:1; Rare:82 | ||||
| chr12:50283433-50283672 | Common:3; Rare:72 |