| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:48852127-48852387 | Common:2; Rare:69 | ||||
| chr12:48925481-48925708 | Common:2; Rare:48 | ||||
| chr12:48957367-48957529 | Common:1; Rare:43 | ||||
| chr12:49018737-49018926 | Rare:78 | ||||
| chr12:49131299-49131617 | Common:2; Rare:125 | ||||
| chr12:49188455-49188590 | Common:1; Rare:19 | ||||
| chr12:49188979-49189281 | Rare:82; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:49264781-49265085 | Common:4; Rare:108 | ||||
| chr12:49568110-49568223 | Common:2; Rare:37 | ||||
| chr12:49741268-49741587 | Rare:87 | ||||
| chr12:49828404-49828573 | Rare:58 | ||||
| chr12:50025439-50025679 | Common:2; Rare:71 | ||||
| chr12:50085295-50085364 | Common:1; Rare:14 | ||||
| chr12:50103897-50104034 | Rare:32 | ||||
| chr12:50112190-50112272 | Rare:24 |