| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:55715965-55716184 | Common:2; Rare:101 | ||||
| chr12:55716358-55716558 | Common:2; Rare:56 | ||||
| chr12:55720315-55720491 | Common:2; Rare:25; Clinvar:3; Clinvar (benign):1 | ||||
| chr12:55728009-55728327 | Common:1; Rare:84 | ||||
| chr12:55728427-55728639 | Rare:38 | ||||
| chr12:55728807-55728866 | Rare:15 | ||||
| chr12:55728940-55729236 | Rare:64 | ||||
| chr12:55729267-55729367 | Rare:18 | ||||
| chr12:55729464-55729816 | Common:2; Rare:70 | ||||
| chr12:55742954-55743423 | Rare:91 | ||||
| chr12:55743483-55743572 | Rare:18 | ||||
| chr12:55743815-55744116 | Rare:49 | ||||
| chr12:55817334-55817416 | Rare:21 | ||||
| chr12:55817652-55818115 | Common:3; Rare:173 | ||||
| chr12:55828906-55829157 | Rare:53 |