| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:76031409-76031769 | Common:1; Rare:127 | ||||
| chr12:76053084-76053352 | Common:1; Rare:68 | ||||
| chr12:76084562-76084786 | Common:1; Rare:75 | ||||
| chr12:76348344-76348534 | Common:1; Rare:71; Clinvar:3; Clinvar (benign):1 | ||||
| chr12:76423260-76423271 | |||||
| chr12:76559641-76559902 | Rare:89 | ||||
| chr12:76764227-76764270 | Rare:16 | ||||
| chr12:76844431-76844669 | Rare:27 | ||||
| chr12:76844677-76845058 | Common:5; Rare:63 | ||||
| chr12:76878948-76879279 | Rare:109 | ||||
| chr12:77065471-77065770 | Common:1; Rare:100 | ||||
| chr12:77940027-77940433 | Common:4; Rare:82 | ||||
| chr12:78864443-78864717 | Common:1; Rare:63 | ||||
| chr12:79597758-79597940 | Common:1; Rare:32 | ||||
| chr12:79690435-79690703 | Common:1; Rare:79 |