| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:213284238-213284504 | Rare:88 | ||||
| chr2:214411040-214411477 | Rare:83 | ||||
| chr2:215311852-215312137 | Common:8; Rare:107 | ||||
| chr2:215436048-215436228 | Common:2; Rare:65 | ||||
| chr2:216081737-216081955 | Common:1; Rare:72 | ||||
| chr2:216372051-216372272 | Rare:26 | ||||
| chr2:216412272-216412534 | Common:2; Rare:58; Clinvar (benign):1 | ||||
| chr2:216498721-216499080 | Common:13; Rare:133 | ||||
| chr2:216694576-216694656 | Rare:18 | ||||
| chr2:218216966-218217226 | Common:2; Rare:93 | ||||
| chr2:218269713-218269785 | Rare:19 | ||||
| chr2:218270048-218270538 | Common:5; Rare:152; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:218292496-218292626 | Common:1; Rare:37 | ||||
| chr2:218568276-218568957 | Common:5; Rare:179 | ||||
| chr2:218659350-218659779 | Common:4; Rare:109 |