| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:751154-751520 | Common:1; Rare:94 | ||||
| chr12:754232-754414 | Common:5; Rare:34; Clinvar (benign):4 | ||||
| chr12:795237-795530 | Common:1; Rare:70 | ||||
| chr12:948870-948908 | Common:1; Rare:9 | ||||
| chr12:1080559-1080717 | Rare:29 | ||||
| chr12:1099286-1099443 | Common:1; Rare:27 | ||||
| chr12:1108357-1108530 | Common:1; Rare:21 | ||||
| chr12:1423020-1423314 | Common:2; Rare:50 | ||||
| chr12:1531400-1531531 | Common:1; Rare:31 | ||||
| chr12:1532182-1532353 | Common:1; Rare:29 | ||||
| chr12:1533141-1533200 | Rare:13 | ||||
| chr12:1533657-1533863 | Common:2; Rare:36 | ||||
| chr12:1534035-1534190 | Common:1; Rare:31 | ||||
| chr12:1534809-1535009 | Common:1; Rare:50 | ||||
| chr12:1554480-1554805 | Common:3; Rare:54 |