| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:49018736-49018943 | Common:1; Rare:87 | ||||
| chr12:49059642-49059920 | Rare:58 | ||||
| chr12:49110654-49111045 | Rare:87 | ||||
| chr12:49130604-49130914 | Common:4; Rare:93 | ||||
| chr12:49131298-49131621 | Common:2; Rare:126 | ||||
| chr12:49186660-49187067 | Common:1; Rare:53; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:49188488-49188630 | Common:2; Rare:19 | ||||
| chr12:49188981-49189384 | Rare:102; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:49264841-49265183 | Common:1; Rare:135 | ||||
| chr12:49269638-49269968 | Common:3; Rare:107 | ||||
| chr12:49322964-49323309 | Common:3; Rare:86 | ||||
| chr12:49366731-49367021 | Common:1; Rare:79 | ||||
| chr12:49367179-49367586 | Common:1; Rare:111 | ||||
| chr12:49568087-49568234 | Common:2; Rare:51 | ||||
| chr12:49623279-49623579 | Common:1; Rare:85 |