| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:186505330-186505521 | Rare:36 | ||||
| chr2:186589907-186590073 | Rare:50 | ||||
| chr2:186590101-186590523 | Rare:141 | ||||
| chr2:187520322-187520568 | Rare:45 | ||||
| chr2:188291700-188291987 | Common:3; Rare:77 | ||||
| chr2:188292554-188292844 | Common:1; Rare:65 | ||||
| chr2:188293005-188293064 | Rare:7 | ||||
| chr2:189441128-189441511 | Common:2; Rare:117 | ||||
| chr2:189783965-189784104 | Common:3; Rare:49; Clinvar (benign):1 | ||||
| chr2:189784268-189784543 | Common:4; Rare:103; Clinvar:8; Clinvar (benign):3 | ||||
| chr2:190343873-190344020 | Rare:28 | ||||
| chr2:190534651-190534882 | Common:1; Rare:73 | ||||
| chr2:190648844-190649125 | Common:2; Rare:90 | ||||
| chr2:190880521-190880900 | Common:4; Rare:124 | ||||
| chr2:190881051-190881333 | Common:1; Rare:111 |