| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:122860504-122861037 | Common:4; Rare:222 | ||||
| chr12:122975188-122975248 | Rare:20 | ||||
| chr12:122980571-122980743 | Common:1; Rare:56 | ||||
| chr12:123233096-123233497 | Common:2; Rare:136; Clinvar:1 | ||||
| chr12:123364725-123364983 | Common:5; Rare:116 | ||||
| chr12:123389923-123390084 | Common:1; Rare:49 | ||||
| chr12:123584396-123584759 | Common:4; Rare:137 | ||||
| chr12:123602023-123602184 | Common:3; Rare:59 | ||||
| chr12:123633611-123633872 | Common:2; Rare:127; Clinvar:8; Clinvar (benign):1 | ||||
| chr12:123712240-123712589 | Common:4; Rare:125; Clinvar:3; Clinvar (benign):3 | ||||
| chr12:123972580-123972656 | Common:3; Rare:24 | ||||
| chr12:124430742-124430973 | Common:1; Rare:83 | ||||
| chr12:124913848-124914199 | Common:9; Rare:136 | ||||
| chr12:124914820-124914993 | Common:2; Rare:61 | ||||
| chr12:131710779-131711119 | Rare:95 |