| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:109154557-109154686 | Common:1; Rare:34 | ||||
| chr12:109477275-109477643 | Common:3; Rare:93 | ||||
| chr12:109573432-109573813 | Common:3; Rare:125; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr12:109900177-109900348 | Rare:63 | ||||
| chr12:110502058-110502217 | Common:1; Rare:58 | ||||
| chr12:111685951-111686085 | Rare:48 | ||||
| chr12:111841894-111842239 | Common:3; Rare:96 | ||||
| chr12:112013129-112013460 | Common:1; Rare:114 | ||||
| chr12:112108761-112108906 | Common:1; Rare:35 | ||||
| chr12:113185435-113185748 | Common:7; Rare:118 | ||||
| chr12:118135955-118136190 | Common:2; Rare:73 | ||||
| chr12:118372887-118373144 | Common:1; Rare:58 | ||||
| chr12:120116725-120116926 | Common:2; Rare:65 | ||||
| chr12:120194690-120194798 | Rare:39 | ||||
| chr12:120201081-120201366 | Common:2; Rare:90 |