| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:207166033-207166427 | Common:3; Rare:146 | ||||
| chr2:207529801-207530108 | Common:2; Rare:84 | ||||
| chr2:207625176-207625515 | Common:1; Rare:94 | ||||
| chr2:207711316-207711652 | Common:1; Rare:100 | ||||
| chr2:208025469-208025620 | Common:1; Rare:41 | ||||
| chr2:208254066-208254224 | Common:1; Rare:27 | ||||
| chr2:208254232-208254483 | Rare:64 | ||||
| chr2:208255019-208255259 | Common:2; Rare:64 | ||||
| chr2:208266032-208266306 | Common:9; Rare:98; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:210002433-210002670 | Common:6; Rare:84 | ||||
| chr2:210476618-210476867 | Common:3; Rare:71 | ||||
| chr2:210477506-210477720 | Rare:62 | ||||
| chr2:212538569-212538887 | Common:1; Rare:98 | ||||
| chr2:212539130-212539455 | Common:7; Rare:61 | ||||
| chr2:213284238-213284490 | Rare:82 |