| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6568234-6568382 | Rare:55 | ||||
| chr12:6606369-6606717 | Common:3; Rare:129 | ||||
| chr12:6607311-6607502 | Rare:61 | ||||
| chr12:6688862-6689089 | Rare:71 | ||||
| chr12:6689329-6689631 | Common:3; Rare:95 | ||||
| chr12:6723943-6724135 | Rare:47 | ||||
| chr12:6724199-6724296 | Rare:21 | ||||
| chr12:6753055-6753189 | Common:4; Rare:49 | ||||
| chr12:6851243-6851497 | Rare:60 | ||||
| chr12:6851902-6852181 | Rare:73 | ||||
| chr12:6867365-6867555 | Common:2; Rare:82; Clinvar:1; Clinvar (benign):2 | ||||
| chr12:6869101-6869387 | Rare:91; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):3 | ||||
| chr12:6873292-6873534 | Common:1; Rare:72 | ||||
| chr12:6914335-6914624 | Rare:69 | ||||
| chr12:6943516-6943817 | Common:4; Rare:126 |