| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:48957367-48957565 | Common:2; Rare:54 | ||||
| chr12:49018736-49018894 | Rare:65 | ||||
| chr12:49131355-49131609 | Common:2; Rare:94 | ||||
| chr12:49188949-49189139 | Rare:61; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:49568104-49568221 | Common:2; Rare:38 | ||||
| chr12:49828390-49828537 | Common:1; Rare:52 | ||||
| chr12:50167297-50167606 | Common:3; Rare:93 | ||||
| chr12:50283452-50283672 | Common:3; Rare:68 | ||||
| chr12:50763948-50764120 | Common:1; Rare:49 | ||||
| chr12:51238648-51238914 | Common:8; Rare:115 | ||||
| chr12:52051143-52051530 | Common:1; Rare:126 | ||||
| chr12:52949802-52950019 | Rare:47 | ||||
| chr12:53006145-53006485 | Common:4; Rare:123 | ||||
| chr12:53048888-53049221 | Common:1; Rare:73 | ||||
| chr12:53079350-53079559 | Common:2; Rare:70 |