| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6200623-6200794 | Common:1; Rare:34 | ||||
| chr12:6330579-6330948 | Common:1; Rare:101; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr12:6375188-6375394 | Common:2; Rare:45 | ||||
| chr12:6375413-6375462 | Rare:8 | ||||
| chr12:6383957-6384340 | Common:2; Rare:93 | ||||
| chr12:6451785-6452159 | Common:4; Rare:70 | ||||
| chr12:6493230-6493398 | Common:6; Rare:47 | ||||
| chr12:6493767-6494148 | Common:2; Rare:111 | ||||
| chr12:6534284-6534602 | Common:5; Rare:130 | ||||
| chr12:6568234-6568388 | Rare:59 | ||||
| chr12:6592489-6592708 | Rare:46 | ||||
| chr12:6601436-6601742 | Rare:70 | ||||
| chr12:6663093-6663289 | Rare:60 | ||||
| chr12:6688887-6689383 | Rare:151 | ||||
| chr12:6689445-6689755 | Common:2; Rare:79 |