| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:108731459-108731657 | Common:2; Rare:74 | ||||
| chr12:109458159-109458431 | Common:4; Rare:39 | ||||
| chr12:109477275-109477439 | Common:3; Rare:62 | ||||
| chr12:109573463-109573866 | Common:3; Rare:123; Clinvar:6; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
| chr12:110450271-110450490 | Common:2; Rare:71 | ||||
| chr12:111685912-111686103 | Rare:66 | ||||
| chr12:111841915-111842267 | Common:2; Rare:100 | ||||
| chr12:112013128-112013496 | Common:1; Rare:135 | ||||
| chr12:113185440-113185777 | Common:8; Rare:119 | ||||
| chr12:116737997-116738336 | Common:5; Rare:113 | ||||
| chr12:118061095-118061286 | Common:1; Rare:49 | ||||
| chr12:118135955-118136199 | Common:2; Rare:75 | ||||
| chr12:118372749-118373193 | Common:2; Rare:114 | ||||
| chr12:120116734-120116917 | Rare:56 | ||||
| chr12:120201068-120201366 | Common:2; Rare:96 |