| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:110124831-110124883 | Rare:3 | ||||
| chr12:110280987-110281215 | Common:1; Rare:87 | ||||
| chr12:110450253-110450490 | Common:2; Rare:83 | ||||
| chr12:110468667-110468915 | Rare:62 | ||||
| chr12:110502047-110502244 | Common:1; Rare:69 | ||||
| chr12:110614008-110614242 | Rare:75; Clinvar:3; Clinvar (benign):2 | ||||
| chr12:110742825-110743183 | Common:3; Rare:137 | ||||
| chr12:111597574-111597897 | Rare:86 | ||||
| chr12:111599338-111599635 | Common:2; Rare:97 | ||||
| chr12:111685730-111686127 | Rare:144 | ||||
| chr12:111766814-111766987 | Rare:54 | ||||
| chr12:111841835-111842243 | Common:3; Rare:114 | ||||
| chr12:112013100-112013472 | Common:1; Rare:133 | ||||
| chr12:112108514-112108818 | Common:2; Rare:83 | ||||
| chr12:112125341-112125583 | Rare:65 |