| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:2876949-2877271 | Rare:100 | ||||
| chr12:2890697-2890938 | Common:1; Rare:97 | ||||
| chr12:3077236-3077439 | Common:7; Rare:88 | ||||
| chr12:3873348-3873514 | Common:1; Rare:39 | ||||
| chr12:4275433-4275590 | Common:2; Rare:24 | ||||
| chr12:4320947-4321253 | Common:5; Rare:115 | ||||
| chr12:4538440-4538727 | Rare:61 | ||||
| chr12:4649045-4649149 | Common:1; Rare:43; Clinvar (benign):1 | ||||
| chr12:6200005-6200559 | Common:4; Rare:166 | ||||
| chr12:6375288-6375624 | Common:4; Rare:84; Clinvar:1; Clinvar (benign):5 | ||||
| chr12:6451795-6452119 | Common:4; Rare:59 | ||||
| chr12:6493087-6493381 | Common:7; Rare:87 | ||||
| chr12:6493770-6494140 | Common:2; Rare:110 | ||||
| chr12:6534326-6534568 | Common:5; Rare:105 | ||||
| chr12:6568249-6568384 | Rare:52 |