Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr9:83219209-83219345 | Common:2; Rare:35 | ||||
chr9:86303127-86303457 | Rare:61 | ||||
chr9:91163192-91163468 | Rare:44 | ||||
chr9:93550538-93550618 | Rare:19 | ||||
chr9:95086022-95086261 | Common:1; Rare:69 | ||||
chr9:95509241-95509379 | Rare:35 | ||||
chr9:96686913-96687057 | Common:2; Rare:45 | ||||
chr9:104784366-104784645 | Common:2; Rare:70; Clinvar (benign):1 | ||||
chr9:107637720-107638004 | Common:1; Rare:65 | ||||
chr9:109058126-109058376 | Common:1; Rare:60 | ||||
chr9:111039190-111039452 | Common:2; Rare:52 | ||||
chr9:112453714-112454018 | Common:2; Rare:42 | ||||
chr9:114398452-114398691 | Common:2; Rare:62 | ||||
chr9:121320509-121320564 | Rare:15 | ||||
chr9:121324310-121324644 | Common:1; Rare:72 |