| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:4011560-4011990 | Common:7; Rare:103 | ||||
| chr12:4015150-4015810 | Common:8; Rare:184 | ||||
| chr12:4025686-4026091 | Common:6; Rare:209 | ||||
| chr12:4228174-4228352 | Common:1; Rare:56 | ||||
| chr12:4269250-4269510 | Common:1; Rare:72 | ||||
| chr12:6295010-6295500 | Rare:144 | ||||
| chr12:6335336-6335799 | Common:3; Rare:113 | ||||
| chr12:6336501-6336901 | Common:1; Rare:113 | ||||
| chr12:6372500-6372830 | Common:3; Rare:99 | ||||
| chr12:6542260-6542600 | Common:5; Rare:99 | ||||
| chr12:6614072-6614934 | Common:1; Rare:309 | ||||
| chr12:6769702-6770670 | Common:3; Rare:373 | ||||
| chr12:6890977-6891440 | Common:7; Rare:293 | ||||
| chr12:6961790-6962401 | Common:4; Rare:178 | ||||
| chr12:6974101-6974570 | Rare:234; Clinvar (pathogenic):2 |