| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:56688090-56688573 | Common:5; Rare:167 | ||||
| chr12:56752321-56752492 | Rare:51 | ||||
| chr12:57111139-57111424 | Common:4; Rare:51 | ||||
| chr12:57230014-57230218 | Rare:42 | ||||
| chr12:57720491-57720930 | Common:1; Rare:111 | ||||
| chr12:57772081-57772230 | Rare:56 | ||||
| chr12:58920156-58920397 | Common:1; Rare:72 | ||||
| chr12:58920496-58920653 | Common:2; Rare:55 | ||||
| chr12:62260194-62260407 | Common:1; Rare:75 | ||||
| chr12:64759119-64759506 | Common:1; Rare:121; Clinvar:6; Clinvar (benign):2 | ||||
| chr12:65824730-65824855 | Common:6; Rare:35 | ||||
| chr12:70243657-70243756 | Common:1; Rare:31 | ||||
| chr12:71663779-71663993 | Common:1; Rare:67 | ||||
| chr12:76031586-76031828 | Common:1; Rare:84 | ||||
| chr12:76348362-76348521 | Common:1; Rare:58; Clinvar:2; Clinvar (benign):1 |