| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:47757954-47758270 | Common:2; Rare:83 | ||||
| chr12:47758701-47759011 | Common:1; Rare:57 | ||||
| chr12:47773114-47773306 | Rare:77 | ||||
| chr12:47819856-47820123 | Common:2; Rare:63 | ||||
| chr12:47820561-47820868 | Rare:43 | ||||
| chr12:47905007-47905117 | Common:1; Rare:24 | ||||
| chr12:48105846-48105938 | Rare:21 | ||||
| chr12:48105977-48106206 | Common:2; Rare:74 | ||||
| chr12:48119190-48119388 | Common:2; Rare:39; Clinvar:4; Clinvar (benign):2 | ||||
| chr12:48350777-48350963 | Rare:66 | ||||
| chr12:48818444-48818512 | Rare:21 | ||||
| chr12:49018736-49018851 | Rare:55 | ||||
| chr12:49130604-49130919 | Common:4; Rare:94 | ||||
| chr12:49131299-49131621 | Common:2; Rare:126 | ||||
| chr12:49188462-49188611 | Common:2; Rare:19 |