| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6568246-6568384 | Rare:53 | ||||
| chr12:6689453-6689732 | Common:2; Rare:70 | ||||
| chr12:6851885-6852174 | Rare:73 | ||||
| chr12:6867355-6867569 | Common:2; Rare:102; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:6914446-6914636 | Rare:53 | ||||
| chr12:6943531-6943820 | Common:4; Rare:120 | ||||
| chr12:6970640-6970961 | Common:3; Rare:102 | ||||
| chr12:8914366-8914696 | Common:6; Rare:95 | ||||
| chr12:8949595-8949862 | Common:1; Rare:53 | ||||
| chr12:10613528-10613638 | Rare:45 | ||||
| chr12:11171565-11171589 | Common:1; Rare:8 | ||||
| chr12:11171604-11171687 | Common:1; Rare:25 | ||||
| chr12:12611782-12611939 | Common:2; Rare:47 | ||||
| chr12:12891504-12891573 | Rare:16 | ||||
| chr12:13000204-13000452 | Common:1; Rare:82 |