| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:19129523-19129830 | Common:2; Rare:141 | ||||
| chr12:19130516-19130745 | Rare:52 | ||||
| chr12:19130748-19130785 | Rare:9 | ||||
| chr12:19439336-19439735 | Common:3; Rare:149 | ||||
| chr12:20369548-20370244 | Common:4; Rare:286 | ||||
| chr12:21437553-21437714 | Common:6; Rare:56 | ||||
| chr12:21501556-21501862 | Common:2; Rare:78 | ||||
| chr12:21527900-21528134 | Common:2; Rare:56 | ||||
| chr12:21657719-21657997 | Common:4; Rare:91; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:21774589-21775067 | Rare:94 | ||||
| chr12:21940927-21941455 | Rare:106 | ||||
| chr12:21941459-21941482 | Rare:4 | ||||
| chr12:21941814-21941992 | Common:3; Rare:39 | ||||
| chr12:22544142-22544260 | Rare:55 | ||||
| chr12:22544470-22544570 | Common:1; Rare:28 |