| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:131929792-131930070 | Common:1; Rare:112; Clinvar:4; Clinvar (benign):4 | ||||
| chr12:131949612-131950003 | Common:2; Rare:126 | ||||
| chr12:132084076-132084374 | Common:6; Rare:102 | ||||
| chr12:132144269-132144516 | Common:2; Rare:99 | ||||
| chr12:132489801-132490219 | Common:4; Rare:129 | ||||
| chr12:132559877-132560047 | Rare:59 | ||||
| chr12:132687296-132687673 | Common:3; Rare:139; Clinvar:10; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
| chr12:132710512-132710930 | Common:5; Rare:148 | ||||
| chr12:132711212-132711334 | Common:2; Rare:26 | ||||
| chr12:132761167-132761351 | Common:3; Rare:47 | ||||
| chr12:132761782-132762366 | Common:6; Rare:208 | ||||
| chr12:132828592-132828625 | Rare:11 | ||||
| chr12:132828769-132828886 | Common:2; Rare:54 | ||||
| chr12:132829018-132829261 | Rare:105 | ||||
| chr12:132887535-132887940 | Common:1; Rare:122 |