| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:74537753-74537868 | Common:1; Rare:44 | ||||
| chr12:75390891-75391105 | Common:1; Rare:66 | ||||
| chr12:75480576-75480904 | Rare:66 | ||||
| chr12:75511525-75511784 | Rare:85 | ||||
| chr12:76030930-76031326 | Common:4; Rare:143 | ||||
| chr12:76031592-76031704 | Common:1; Rare:38 | ||||
| chr12:76053089-76053234 | Common:1; Rare:45 | ||||
| chr12:76083832-76084070 | Rare:65 | ||||
| chr12:76084547-76084857 | Common:1; Rare:101 | ||||
| chr12:76085015-76085065 | Common:2; Rare:11 | ||||
| chr12:76348332-76348468 | Common:1; Rare:55; Clinvar:3; Clinvar (benign):1 | ||||
| chr12:76559696-76559884 | Rare:75 | ||||
| chr12:76764040-76764272 | Common:2; Rare:94 | ||||
| chr12:76879008-76879169 | Rare:49 | ||||
| chr12:77065485-77065885 | Common:3; Rare:126 |