| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:49188981-49189296 | Rare:88; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:49264749-49265152 | Common:5; Rare:147 | ||||
| chr12:49269544-49269917 | Common:4; Rare:117 | ||||
| chr12:49322980-49323313 | Common:3; Rare:78 | ||||
| chr12:49367256-49367524 | Common:1; Rare:73 | ||||
| chr12:49568098-49568443 | Common:2; Rare:80 | ||||
| chr12:49828387-49828571 | Common:1; Rare:66 | ||||
| chr12:50025412-50025764 | Common:2; Rare:97 | ||||
| chr12:50085296-50085363 | Common:1; Rare:12 | ||||
| chr12:50283500-50283652 | Common:1; Rare:46 | ||||
| chr12:51270267-51270427 | Common:3; Rare:46 | ||||
| chr12:51391611-51391736 | Common:1; Rare:39 | ||||
| chr12:52905036-52905320 | Common:3; Rare:65 | ||||
| chr12:53079362-53079516 | Common:2; Rare:54 | ||||
| chr12:53252049-53252203 | Common:3; Rare:59 |