| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:72274893-72275112 | Rare:31 | ||||
| chr12:74537717-74537884 | Common:1; Rare:65 | ||||
| chr12:75390876-75391109 | Common:1; Rare:70 | ||||
| chr12:76053211-76053548 | Rare:68 | ||||
| chr12:76348360-76348520 | Common:1; Rare:59; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:76486048-76486275 | Rare:39 | ||||
| chr12:76559511-76559915 | Common:2; Rare:133 | ||||
| chr12:76763965-76764313 | Common:3; Rare:150 | ||||
| chr12:79690506-79690670 | Rare:50 | ||||
| chr12:79690944-79691246 | Common:1; Rare:105 | ||||
| chr12:79934704-79935301 | Common:1; Rare:206 | ||||
| chr12:79935342-79935369 | Rare:6 | ||||
| chr12:80937670-80937843 | Common:1; Rare:54 | ||||
| chr12:81077973-81078123 | Rare:36 | ||||
| chr12:82358273-82358555 | Common:1; Rare:134 |