| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:49188488-49188607 | Common:2; Rare:17 | ||||
| chr12:49188981-49189336 | Rare:92; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:49264775-49265092 | Common:4; Rare:113 | ||||
| chr12:49322964-49323297 | Common:3; Rare:79 | ||||
| chr12:49568104-49568253 | Common:2; Rare:46 | ||||
| chr12:49623295-49623571 | Common:1; Rare:76 | ||||
| chr12:49828364-49828626 | Common:1; Rare:97 | ||||
| chr12:50283452-50283678 | Common:3; Rare:71 | ||||
| chr12:50400789-50401008 | Common:1; Rare:74 | ||||
| chr12:50763925-50764120 | Common:1; Rare:56 | ||||
| chr12:51238686-51238914 | Common:3; Rare:95 | ||||
| chr12:51270277-51270367 | Common:3; Rare:24 | ||||
| chr12:52051152-52051530 | Common:1; Rare:124 | ||||
| chr12:52249123-52249306 | Rare:38 | ||||
| chr12:52520364-52520606 | Common:2; Rare:56; Clinvar:2; Clinvar (benign):2 |