| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:27263001-27263220 | Rare:55 | ||||
| chr2:27264092-27264140 | Rare:11 | ||||
| chr2:27282235-27282510 | Rare:39 | ||||
| chr2:27322890-27323242 | Common:2; Rare:107; Clinvar (benign):1 | ||||
| chr2:27323308-27323428 | Common:1; Rare:32 | ||||
| chr2:27323575-27323785 | Rare:33 | ||||
| chr2:27356078-27356308 | Common:1; Rare:64 | ||||
| chr2:27356384-27356674 | Rare:103 | ||||
| chr2:27356693-27356887 | Common:1; Rare:51 | ||||
| chr2:27356952-27357365 | Common:2; Rare:124 | ||||
| chr2:27369794-27370018 | Rare:85; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:27370237-27370729 | Common:2; Rare:200 | ||||
| chr2:27371148-27371315 | Common:1; Rare:49 | ||||
| chr2:27379791-27379999 | Common:3; Rare:43 | ||||
| chr2:27380682-27381012 | Common:1; Rare:120; Clinvar:2 |