| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:108562361-108562686 | Common:9; Rare:130; Clinvar:2; Clinvar (benign):6 | ||||
| chr12:108633641-108633993 | Rare:69 | ||||
| chr12:109093399-109093719 | Common:3; Rare:113 | ||||
| chr12:109097867-109098204 | Common:4; Rare:105 | ||||
| chr12:109477293-109477666 | Common:3; Rare:90 | ||||
| chr12:109573472-109573825 | Common:3; Rare:105; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr12:109880426-109880675 | Common:1; Rare:68 | ||||
| chr12:109900202-109900356 | Rare:62 | ||||
| chr12:109996206-109996436 | Common:2; Rare:66 | ||||
| chr12:109999099-109999213 | Rare:17 | ||||
| chr12:110049151-110049229 | Rare:16 | ||||
| chr12:110450254-110450456 | Common:2; Rare:73 | ||||
| chr12:110468199-110468525 | Common:3; Rare:109 | ||||
| chr12:110468697-110468909 | Rare:56 | ||||
| chr12:110502047-110502340 | Common:1; Rare:109 |