| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:183124252-183124457 | Common:4; Rare:71 | ||||
| chr2:184598314-184598385 | Rare:22 | ||||
| chr2:186485966-186486374 | Common:3; Rare:117 | ||||
| chr2:186590070-186590335 | Rare:81 | ||||
| chr2:186693914-186694291 | Common:2; Rare:148 | ||||
| chr2:188291593-188292088 | Common:7; Rare:142 | ||||
| chr2:188292706-188292863 | Common:1; Rare:38 | ||||
| chr2:188974352-188974564 | Rare:60; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr2:189441038-189441504 | Common:3; Rare:144 | ||||
| chr2:189783965-189784111 | Common:3; Rare:53; Clinvar (benign):1 | ||||
| chr2:189784275-189784543 | Common:4; Rare:98; Clinvar:8; Clinvar (benign):2 | ||||
| chr2:190343886-190343931 | Rare:4 | ||||
| chr2:190534696-190534913 | Common:1; Rare:69 | ||||
| chr2:190648695-190648906 | Common:1; Rare:80 | ||||
| chr2:190880626-190880897 | Common:4; Rare:90 |