| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:132687275-132687713 | Common:4; Rare:159; Clinvar:12; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
| chr12:132710472-132710903 | Common:5; Rare:152 | ||||
| chr12:132711204-132711304 | Common:1; Rare:21 | ||||
| chr12:132761162-132761365 | Common:3; Rare:57 | ||||
| chr12:132761748-132762424 | Common:6; Rare:233 | ||||
| chr12:132828596-132828661 | Rare:17 | ||||
| chr12:132828785-132829294 | Common:4; Rare:193 | ||||
| chr12:132887529-132888106 | Common:2; Rare:161 | ||||
| chr12:132955813-132956125 | Common:3; Rare:40 | ||||
| chr12:132956258-132956490 | Common:2; Rare:48 | ||||
| chr12:132986143-132986505 | Rare:95 | ||||
| chr12:133037056-133037403 | Common:4; Rare:65 | ||||
| chr12:133037473-133037623 | Rare:50 | ||||
| chr12:133037727-133037831 | Common:2; Rare:23 | ||||
| chr12:133080026-133080518 | Common:9; Rare:151 |