| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:58573020-58573131 | Rare:37 | ||||
| chr19:58573298-58573711 | Common:3; Rare:104 | ||||
| chr2:264030-264121 | Common:1; Rare:30 | ||||
| chr2:264555-265011 | Common:4; Rare:182 | ||||
| chr2:676654-677133 | Common:3; Rare:114 | ||||
| chr2:677338-677558 | Common:1; Rare:95 | ||||
| chr2:1654387-1654670 | Common:1; Rare:75; Clinvar (benign):1 | ||||
| chr2:1744267-1744405 | Common:1; Rare:42 | ||||
| chr2:1744409-1744638 | Common:1; Rare:76 | ||||
| chr2:3377690-3377953 | Rare:75 | ||||
| chr2:3454977-3455295 | Common:3; Rare:92 | ||||
| chr2:3472234-3472520 | Common:3; Rare:80 | ||||
| chr2:3478690-3479469 | Common:6; Rare:250; Clinvar (pathogenic):1 | ||||
| chr2:3519370-3519674 | Common:3; Rare:87 | ||||
| chr2:3558225-3558715 | Common:6; Rare:183 |