| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:48122458-48122717 | Common:2; Rare:30 | ||||
| chr12:48350796-48350963 | Rare:61 | ||||
| chr12:49018741-49018861 | Rare:52 | ||||
| chr12:49131341-49131606 | Common:2; Rare:105 | ||||
| chr12:49188492-49188557 | Common:1; Rare:10 | ||||
| chr12:49188981-49189274 | Rare:81; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:49322980-49323277 | Common:2; Rare:67 | ||||
| chr12:49568104-49568205 | Common:2; Rare:36 | ||||
| chr12:49828387-49828553 | Common:1; Rare:59 | ||||
| chr12:50085287-50085358 | Rare:16 | ||||
| chr12:50283452-50283672 | Common:3; Rare:68 | ||||
| chr12:51048129-51048370 | Common:1; Rare:87 | ||||
| chr12:51238648-51238899 | Common:8; Rare:111 | ||||
| chr12:51270277-51270344 | Common:2; Rare:18 | ||||
| chr12:52051152-52051478 | Common:1; Rare:108 |