| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:48939694-48940079 | Common:2; Rare:89 | ||||
| chr12:48957345-48957581 | Common:2; Rare:68 | ||||
| chr12:49018705-49018947 | Common:1; Rare:104 | ||||
| chr12:49069934-49070160 | Common:2; Rare:56 | ||||
| chr12:49110661-49111064 | Rare:91 | ||||
| chr12:49131282-49131667 | Common:2; Rare:152 | ||||
| chr12:49188506-49188607 | Common:2; Rare:15 | ||||
| chr12:49188979-49189296 | Rare:88; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:49264749-49265208 | Common:6; Rare:168 | ||||
| chr12:49269639-49269937 | Common:3; Rare:95 | ||||
| chr12:49322963-49323323 | Common:3; Rare:88 | ||||
| chr12:49366785-49367021 | Common:1; Rare:60 | ||||
| chr12:49367183-49367548 | Common:1; Rare:103 | ||||
| chr12:49568072-49568453 | Common:2; Rare:95 | ||||
| chr12:49623247-49623579 | Common:2; Rare:95 |