| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:71663813-71664042 | Common:1; Rare:65 | ||||
| chr12:71664093-71664454 | Rare:94 | ||||
| chr12:71686040-71686113 | Common:1; Rare:20 | ||||
| chr12:74537717-74537884 | Common:1; Rare:65 | ||||
| chr12:75390886-75391109 | Common:1; Rare:69 | ||||
| chr12:76030900-76031190 | Common:4; Rare:123 | ||||
| chr12:76084568-76084799 | Common:1; Rare:77 | ||||
| chr12:76348403-76348545 | Common:2; Rare:46; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:76559558-76559893 | Common:2; Rare:115 | ||||
| chr12:76764010-76764276 | Common:2; Rare:108 | ||||
| chr12:76878967-76879133 | Rare:54 | ||||
| chr12:78864593-78865069 | Common:2; Rare:105 | ||||
| chr12:79934886-79935349 | Common:1; Rare:178 | ||||
| chr12:79935351-79935369 | Rare:5 | ||||
| chr12:80937679-80937813 | Common:1; Rare:40 |