| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:27217222-27217504 | Rare:106 | ||||
| chr2:27217519-27217539 | Rare:10 | ||||
| chr2:27322990-27323117 | Rare:38; Clinvar (benign):1 | ||||
| chr2:27356175-27356286 | Rare:26 | ||||
| chr2:27356750-27356907 | Rare:39 | ||||
| chr2:27356973-27357199 | Common:2; Rare:82 | ||||
| chr2:27370310-27370648 | Common:1; Rare:133 | ||||
| chr2:27442189-27442410 | Common:1; Rare:72 | ||||
| chr2:27496697-27496905 | Rare:42 | ||||
| chr2:27582967-27583127 | Rare:59 | ||||
| chr2:27628981-27629090 | Common:1; Rare:58 | ||||
| chr2:27663362-27663487 | Rare:30 | ||||
| chr2:27663503-27663934 | Rare:151 | ||||
| chr2:27771548-27771812 | Common:1; Rare:89 | ||||
| chr2:27890346-27890839 | Common:1; Rare:136 |