| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:49264781-49265117 | Common:4; Rare:124 | ||||
| chr12:49322964-49323303 | Common:3; Rare:82 | ||||
| chr12:49367212-49367534 | Common:1; Rare:89 | ||||
| chr12:49568104-49568216 | Common:2; Rare:37 | ||||
| chr12:49623367-49623579 | Rare:49 | ||||
| chr12:49828359-49828543 | Common:1; Rare:69 | ||||
| chr12:50085061-50085399 | Common:1; Rare:92 | ||||
| chr12:50283452-50283672 | Common:3; Rare:68 | ||||
| chr12:50763937-50764349 | Common:1; Rare:109 | ||||
| chr12:50924470-50924755 | Common:3; Rare:82 | ||||
| chr12:51026271-51026487 | Common:2; Rare:95; Clinvar:3; Clinvar (benign):2 | ||||
| chr12:51048119-51048365 | Common:1; Rare:86 | ||||
| chr12:51173027-51173271 | Rare:45 | ||||
| chr12:51238648-51238914 | Common:8; Rare:115 | ||||
| chr12:51270165-51270427 | Common:4; Rare:70 |