| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:74537684-74537884 | Common:1; Rare:74 | ||||
| chr12:75390898-75391109 | Common:1; Rare:65 | ||||
| chr12:76031593-76031841 | Common:1; Rare:82 | ||||
| chr12:76348391-76348490 | Common:1; Rare:33; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:76559696-76559893 | Rare:76 | ||||
| chr12:76764040-76764261 | Common:2; Rare:91 | ||||
| chr12:76878954-76879114 | Rare:52 | ||||
| chr12:78864581-78865064 | Common:2; Rare:105 | ||||
| chr12:79934896-79935349 | Common:1; Rare:176 | ||||
| chr12:79935351-79935571 | Common:3; Rare:55 | ||||
| chr12:80937679-80937826 | Common:1; Rare:47 | ||||
| chr12:81758625-81758805 | Rare:35 | ||||
| chr12:81759285-81759522 | Common:3; Rare:52 | ||||
| chr12:82358343-82358556 | Rare:98 | ||||
| chr12:82358733-82358896 | Common:3; Rare:86 |