| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:206765278-206765645 | Common:3; Rare:97; Clinvar:4; Clinvar (benign):4 | ||||
| chr2:207165914-207166142 | Rare:47 | ||||
| chr2:207529687-207530025 | Common:3; Rare:108 | ||||
| chr2:207625226-207625394 | Common:1; Rare:47 | ||||
| chr2:208025480-208025614 | Common:1; Rare:35 | ||||
| chr2:208255024-208255228 | Common:2; Rare:54 | ||||
| chr2:208266032-208266313 | Common:9; Rare:100; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:210002433-210002659 | Common:6; Rare:77 | ||||
| chr2:210225104-210225178 | Rare:19 | ||||
| chr2:215311910-215312140 | Common:8; Rare:95 | ||||
| chr2:215365502-215365874 | Common:5; Rare:95 | ||||
| chr2:215375212-215375725 | Common:2; Rare:138 | ||||
| chr2:215435648-215436152 | Common:3; Rare:124 | ||||
| chr2:216081781-216081866 | Rare:25 | ||||
| chr2:216694438-216694455 | Rare:3 |