| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:66130699-66130801 | Rare:38 | ||||
| chr12:68332356-68332631 | Common:1; Rare:77 | ||||
| chr12:68686839-68687004 | Common:3; Rare:43 | ||||
| chr12:71663800-71663973 | Common:1; Rare:55 | ||||
| chr12:75390893-75391209 | Common:1; Rare:117 | ||||
| chr12:76031586-76031812 | Common:1; Rare:81 | ||||
| chr12:76348365-76348460 | Common:1; Rare:34; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:76559768-76559874 | Rare:48 | ||||
| chr12:76879012-76879235 | Rare:70 | ||||
| chr12:79934935-79935396 | Common:1; Rare:180 | ||||
| chr12:82358343-82358552 | Rare:95 | ||||
| chr12:82358740-82358896 | Common:3; Rare:81 | ||||
| chr12:85279935-85280277 | Common:1; Rare:94 | ||||
| chr12:88142066-88142367 | Rare:83; Clinvar:3 | ||||
| chr12:88580424-88580551 | Common:2; Rare:47 |