| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:62260060-62260427 | Common:1; Rare:133 | ||||
| chr12:63780080-63780175 | Rare:43; Clinvar (pathogenic):1 | ||||
| chr12:64222242-64222357 | Rare:39 | ||||
| chr12:64404241-64404681 | Common:5; Rare:154 | ||||
| chr12:64452041-64452171 | Common:1; Rare:47 | ||||
| chr12:64759373-64759472 | Rare:33; Clinvar:3 | ||||
| chr12:65824212-65824514 | Common:1; Rare:76 | ||||
| chr12:66130703-66130861 | Rare:57 | ||||
| chr12:67269503-67269665 | Rare:48 | ||||
| chr12:68332265-68332615 | Common:1; Rare:115 | ||||
| chr12:68610695-68611041 | Common:1; Rare:148 | ||||
| chr12:68686835-68687040 | Common:3; Rare:62 | ||||
| chr12:68746021-68746226 | Common:3; Rare:70 | ||||
| chr12:68807894-68808243 | Common:4; Rare:103 | ||||
| chr12:68808848-68809034 | Rare:35 |