| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:238288744-238289222 | Rare:182 | ||||
| chr2:238426611-238427150 | Common:7; Rare:163 | ||||
| chr2:238427318-238427592 | Common:4; Rare:69 | ||||
| chr2:239401378-239401491 | Rare:47 | ||||
| chr2:239401581-239401812 | Common:1; Rare:121 | ||||
| chr2:240025281-240025682 | Common:3; Rare:149; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr2:240025863-240026058 | Common:1; Rare:39 | ||||
| chr2:240136234-240136457 | Common:2; Rare:97 | ||||
| chr2:240136539-240136671 | Common:2; Rare:26 | ||||
| chr2:240136777-240136921 | Common:3; Rare:38 | ||||
| chr2:240560215-240560445 | Common:2; Rare:94 | ||||
| chr2:240560676-240560834 | Rare:79 | ||||
| chr2:240560998-240561369 | Common:4; Rare:183 | ||||
| chr2:240561753-240561969 | Common:1; Rare:39 | ||||
| chr2:240565679-240565797 | Rare:25 |