| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:49188980-49189111 | Rare:50; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:49189114-49189216 | Rare:14 | ||||
| chr12:49264781-49265082 | Common:4; Rare:104 | ||||
| chr12:49293167-49293306 | Rare:22 | ||||
| chr12:49367129-49367524 | Common:2; Rare:112 | ||||
| chr12:49568087-49568253 | Common:2; Rare:56 | ||||
| chr12:49828374-49828594 | Common:1; Rare:84 | ||||
| chr12:50085020-50085372 | Common:1; Rare:91 | ||||
| chr12:50283473-50283678 | Common:3; Rare:67 | ||||
| chr12:50763925-50764120 | Common:1; Rare:56 | ||||
| chr12:50924466-50924749 | Common:3; Rare:80 | ||||
| chr12:51048077-51048371 | Common:2; Rare:104 | ||||
| chr12:51238648-51238914 | Common:8; Rare:115 | ||||
| chr12:52051152-52051518 | Common:1; Rare:122 | ||||
| chr12:53006155-53006489 | Common:4; Rare:121 |