| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:123712217-123712518 | Common:3; Rare:108; Clinvar:3; Clinvar (benign):2 | ||||
| chr12:123972575-123972650 | Common:3; Rare:26 | ||||
| chr12:123973004-123973303 | Common:2; Rare:98 | ||||
| chr12:124356782-124356986 | Common:1; Rare:41 | ||||
| chr12:124388796-124388959 | Common:3; Rare:47 | ||||
| chr12:124389302-124389459 | Rare:42 | ||||
| chr12:124914567-124915096 | Common:9; Rare:214 | ||||
| chr12:128824011-128824123 | Common:1; Rare:39 | ||||
| chr12:128852836-128853111 | Common:2; Rare:57 | ||||
| chr12:128853371-128853635 | Common:2; Rare:75 | ||||
| chr12:130839140-130839394 | Common:2; Rare:93 | ||||
| chr12:130871727-130872129 | Common:4; Rare:166 | ||||
| chr12:131710825-131711138 | Common:1; Rare:81 | ||||
| chr12:131929041-131929306 | Common:10; Rare:82; Clinvar:1 | ||||
| chr12:132275222-132275438 | Common:4; Rare:47 |