| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:47773079-47773317 | Rare:218 | ||||
| chr12:47819090-47819570 | Common:3; Rare:128 | ||||
| chr12:47819644-47819798 | Rare:59 | ||||
| chr12:47819799-47820387 | Common:11; Rare:295 | ||||
| chr12:47820369-47820890 | Common:3; Rare:185 | ||||
| chr12:47904902-47905242 | Common:3; Rare:207; Clinvar:3 | ||||
| chr12:47905365-47905536 | Rare:65 | ||||
| chr12:47963379-47963696 | Common:5; Rare:141 | ||||
| chr12:47964130-47964700 | Common:4; Rare:137 | ||||
| chr12:48105310-48105512 | Common:2; Rare:58 | ||||
| chr12:48105806-48105956 | Common:1; Rare:66 | ||||
| chr12:48105921-48106395 | Common:4; Rare:307 | ||||
| chr12:48119137-48119408 | Common:4; Rare:98; Clinvar:8; Clinvar (benign):4 | ||||
| chr12:48156869-48157133 | Common:2; Rare:75 | ||||
| chr12:48157323-48158001 | Common:15; Rare:373 |