| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:128824129-128824167 | Common:1; Rare:13 | ||||
| chr12:130716239-130716422 | Rare:29 | ||||
| chr12:130871741-130872126 | Common:4; Rare:159 | ||||
| chr12:130872346-130872600 | Common:1; Rare:96 | ||||
| chr12:131710839-131711119 | Rare:68 | ||||
| chr12:131908772-131908912 | Rare:68 | ||||
| chr12:131928990-131929301 | Common:10; Rare:93; Clinvar:1 | ||||
| chr12:131949626-131950014 | Common:2; Rare:130 | ||||
| chr12:132144109-132144486 | Common:2; Rare:132 | ||||
| chr12:132559893-132560114 | Rare:75 | ||||
| chr12:132687274-132687651 | Common:2; Rare:137; Clinvar:12; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
| chr12:132710564-132711035 | Common:5; Rare:152 | ||||
| chr12:132828820-132829255 | Common:4; Rare:164 | ||||
| chr12:132887553-132887845 | Rare:85 | ||||
| chr12:132908447-132908742 | Common:3; Rare:72 |