| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:215311879-215312139 | Common:8; Rare:100 | ||||
| chr2:215436037-215436307 | Common:2; Rare:90 | ||||
| chr2:216081761-216081904 | Common:1; Rare:46 | ||||
| chr2:216498719-216498886 | Common:6; Rare:69 | ||||
| chr2:216694638-216694977 | Rare:77 | ||||
| chr2:217905443-217905636 | Rare:41 | ||||
| chr2:217978639-217978672 | Rare:12 | ||||
| chr2:217978773-217978963 | Common:1; Rare:60 | ||||
| chr2:218217086-218217226 | Rare:52 | ||||
| chr2:218270057-218270534 | Common:5; Rare:146; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:218289992-218290059 | Common:2; Rare:13 | ||||
| chr2:218568296-218568665 | Common:3; Rare:98 | ||||
| chr2:218568670-218568966 | Common:1; Rare:79 | ||||
| chr2:218659334-218659738 | Common:4; Rare:95 | ||||
| chr2:218671977-218672334 | Common:2; Rare:89 |