Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:197029779-197029932 | Common:1; Rare:49 | ||||
chr3:197736819-197737128 | Common:3; Rare:95 | ||||
chr3:197749821-197749979 | Rare:67 | ||||
chr3:197949893-197950250 | Common:4; Rare:111; Clinvar (benign):2 | ||||
chr3:197959947-197960248 | Common:1; Rare:104 | ||||
chr4:337544-337861 | Common:1; Rare:87 | ||||
chr4:499123-499307 | Common:3; Rare:73 | ||||
chr4:663605-663725 | Rare:36 | ||||
chr4:674212-674618 | Common:4; Rare:185 | ||||
chr4:681123-681227 | Rare:42 | ||||
chr4:705588-705846 | Rare:84 | ||||
chr4:932250-932487 | Common:2; Rare:93 | ||||
chr4:1113524-1113632 | Common:2; Rare:39 | ||||
chr4:1201526-1201724 | Rare:51 | ||||
chr4:1249988-1250045 | Common:1; Rare:9 |