| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:188291639-188291939 | Common:2; Rare:81 | ||||
| chr2:188292679-188292855 | Common:1; Rare:42 | ||||
| chr2:188293000-188293064 | Rare:7 | ||||
| chr2:189441072-189441438 | Common:1; Rare:97 | ||||
| chr2:189580736-189581010 | Common:1; Rare:88; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:189783965-189784133 | Common:3; Rare:64; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:189784259-189784532 | Common:4; Rare:97; Clinvar:8; Clinvar (benign):3 | ||||
| chr2:190180768-190181092 | Rare:98 | ||||
| chr2:190343834-190343955 | Rare:26 | ||||
| chr2:190534696-190534846 | Common:1; Rare:50 | ||||
| chr2:190881015-190881361 | Common:2; Rare:135 | ||||
| chr2:191246137-191246249 | Rare:42 | ||||
| chr2:191677854-191678218 | Common:4; Rare:103 | ||||
| chr2:191678589-191679010 | Common:1; Rare:137 | ||||
| chr2:191847026-191847104 | Rare:16 |