| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:75480609-75481002 | Rare:92 | ||||
| chr12:75511512-75511779 | Rare:88 | ||||
| chr12:76031578-76031692 | Rare:39 | ||||
| chr12:76031695-76031817 | Rare:45 | ||||
| chr12:76067116-76067471 | Common:5; Rare:71 | ||||
| chr12:76084536-76084668 | Rare:51 | ||||
| chr12:76085019-76085092 | Common:2; Rare:21 | ||||
| chr12:76348360-76348476 | Common:1; Rare:41; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:76559479-76559874 | Common:2; Rare:127 | ||||
| chr12:76763942-76764312 | Common:4; Rare:159 | ||||
| chr12:76844434-76844663 | Rare:25 | ||||
| chr12:76845255-76845412 | Rare:20 | ||||
| chr12:76864984-76865007 | Rare:4 | ||||
| chr12:76879000-76879216 | Rare:67 | ||||
| chr12:77065523-77065680 | Rare:49 |