| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:52492622-52492744 | Common:4; Rare:43; Clinvar:2; Clinvar (pathogenic):3 | ||||
| chr12:52520331-52520598 | Common:2; Rare:60; Clinvar:3; Clinvar (benign):2 | ||||
| chr12:52813595-52814205 | Common:8; Rare:233; Clinvar:7; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
| chr12:52905036-52905347 | Common:3; Rare:68 | ||||
| chr12:53006223-53006486 | Common:2; Rare:97 | ||||
| chr12:53048890-53049203 | Common:1; Rare:70 | ||||
| chr12:53049865-53050086 | Rare:56 | ||||
| chr12:53079365-53079503 | Common:1; Rare:47 | ||||
| chr12:53097343-53097709 | Common:1; Rare:81 | ||||
| chr12:53232174-53232432 | Common:2; Rare:55 | ||||
| chr12:53252013-53252212 | Common:3; Rare:78 | ||||
| chr12:53501224-53501320 | Rare:28 | ||||
| chr12:53727424-53727714 | Rare:65 | ||||
| chr12:55716005-55716186 | Common:1; Rare:87 | ||||
| chr12:55728357-55728498 | Rare:38 |