| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:123436444-123436582 | Rare:26 | ||||
| chr12:123458048-123458204 | Common:1; Rare:36 | ||||
| chr12:123584304-123584813 | Common:9; Rare:172 | ||||
| chr12:123601987-123602184 | Common:3; Rare:67 | ||||
| chr12:123633545-123633877 | Common:2; Rare:157; Clinvar:8; Clinvar (benign):1 | ||||
| chr12:123972537-123972872 | Common:6; Rare:115 | ||||
| chr12:124328056-124328092 | Rare:8 | ||||
| chr12:124422621-124422819 | Common:2; Rare:48 | ||||
| chr12:124863801-124864024 | Common:1; Rare:55 | ||||
| chr12:124913612-124913948 | Common:1; Rare:125 | ||||
| chr12:124914041-124914251 | Common:7; Rare:83 | ||||
| chr12:128823393-128823521 | Rare:43 | ||||
| chr12:128823969-128824148 | Common:2; Rare:69 | ||||
| chr12:131929018-131929507 | Common:10; Rare:140; Clinvar:5 | ||||
| chr12:132144306-132144527 | Common:1; Rare:92 |