| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6237560-6237870 | Common:2; Rare:75 | ||||
| chr12:6267380-6267670 | Common:2; Rare:76 | ||||
| chr12:6277955-6278339 | Common:1; Rare:106 | ||||
| chr12:6323337-6323631 | Common:2; Rare:93 | ||||
| chr12:6326365-6327369 | Common:8; Rare:349 | ||||
| chr12:6330100-6330460 | Common:4; Rare:80; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:6335767-6335899 | Common:2; Rare:50 | ||||
| chr12:6336627-6336865 | Common:1; Rare:77 | ||||
| chr12:6337161-6337561 | Rare:107 | ||||
| chr12:6339264-6339664 | Common:1; Rare:70 | ||||
| chr12:6340090-6340490 | Common:2; Rare:65 | ||||
| chr12:6340716-6341014 | Rare:75 | ||||
| chr12:6367911-6368556 | Common:13; Rare:140 | ||||
| chr12:6426004-6426240 | Common:1; Rare:45 | ||||
| chr12:6426163-6426315 | Common:1; Rare:28 |