| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:110280463-110280716 | Rare:62 | ||||
| chr12:110280951-110281276 | Common:1; Rare:123 | ||||
| chr12:110281774-110281917 | Common:1; Rare:35; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr12:110450254-110450437 | Common:2; Rare:69 | ||||
| chr12:110468715-110468915 | Rare:54 | ||||
| chr12:110502051-110502244 | Common:1; Rare:68 | ||||
| chr12:110583008-110583206 | Common:2; Rare:51 | ||||
| chr12:110742825-110743095 | Common:3; Rare:114 | ||||
| chr12:110920469-110920779 | Common:2; Rare:91; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr12:111369014-111369210 | Common:1; Rare:53 | ||||
| chr12:111599338-111599611 | Common:2; Rare:83 | ||||
| chr12:111685719-111686120 | Rare:141 | ||||
| chr12:111766807-111766985 | Rare:54 | ||||
| chr12:111841851-111842233 | Common:3; Rare:105 | ||||
| chr12:112005954-112006094 | Rare:24 |