| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:130839080-130839490 | Common:4; Rare:126 | ||||
| chr12:130871675-130872117 | Common:4; Rare:182 | ||||
| chr12:130872310-130873236 | Common:4; Rare:450 | ||||
| chr12:131710767-131711105 | Rare:94 | ||||
| chr12:131894427-131894742 | Common:2; Rare:100 | ||||
| chr12:131929045-131929284 | Common:10; Rare:74; Clinvar:1 | ||||
| chr12:131949833-131950017 | Common:1; Rare:69 | ||||
| chr12:132084053-132084323 | Common:6; Rare:89 | ||||
| chr12:132144284-132144477 | Rare:76 | ||||
| chr12:132489800-132490161 | Common:3; Rare:110 | ||||
| chr12:132560045-132560596 | Common:7; Rare:178 | ||||
| chr12:132686651-132687051 | Common:1; Rare:158 | ||||
| chr12:132687311-132687655 | Common:2; Rare:128; Clinvar:5; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
| chr12:132710763-132710882 | Common:3; Rare:49 | ||||
| chr12:132761780-132762268 | Common:3; Rare:178 |