| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:186590141-186590460 | Rare:106 | ||||
| chr2:187554284-187554514 | Rare:47 | ||||
| chr2:188291593-188291939 | Common:4; Rare:96 | ||||
| chr2:188292692-188292869 | Common:1; Rare:44 | ||||
| chr2:188974215-188974609 | Rare:99; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr2:189002857-189003060 | Rare:54; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):4 | ||||
| chr2:189003402-189003966 | Common:4; Rare:132; Clinvar:1; Clinvar (benign):5; Clinvar (pathogenic):7 | ||||
| chr2:189007466-189008146 | Common:2; Rare:182; Clinvar:8; Clinvar (benign):10; Clinvar (pathogenic):24 | ||||
| chr2:189062863-189063072 | Rare:44; Clinvar:2; Clinvar (benign):3 | ||||
| chr2:189441072-189441504 | Common:2; Rare:131 | ||||
| chr2:189783956-189784078 | Common:2; Rare:39 | ||||
| chr2:189784289-189784543 | Common:4; Rare:93; Clinvar:8; Clinvar (benign):2 | ||||
| chr2:190343873-190343931 | Rare:7 | ||||
| chr2:190648709-190648916 | Common:1; Rare:75 | ||||
| chr2:190880644-190880897 | Common:4; Rare:88 |