| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6568234-6568382 | Rare:55 | ||||
| chr12:6723841-6724296 | Common:1; Rare:99 | ||||
| chr12:6851894-6852174 | Rare:72 | ||||
| chr12:6867406-6867561 | Common:2; Rare:73; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:6873334-6873532 | Common:1; Rare:54 | ||||
| chr12:6970616-6970963 | Common:4; Rare:108; Clinvar (benign):1 | ||||
| chr12:7018467-7018707 | Common:1; Rare:65 | ||||
| chr12:7189512-7189711 | Rare:64; Clinvar:1 | ||||
| chr12:8032570-8032751 | Common:4; Rare:65 | ||||
| chr12:8949604-8949855 | Common:1; Rare:49 | ||||
| chr12:9869358-9869591 | Common:3; Rare:37 | ||||
| chr12:10613508-10613686 | Common:1; Rare:70 | ||||
| chr12:11171551-11171749 | Common:3; Rare:70 | ||||
| chr12:12356997-12357098 | Common:1; Rare:51 | ||||
| chr12:12891465-12891567 | Rare:26 |