Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr9:34597252-34597490 | Common:1; Rare:33 | ||||
chr9:35604037-35604282 | Common:3; Rare:68 | ||||
chr9:35706746-35707154 | Common:2; Rare:115 | ||||
chr9:35714253-35714531 | Common:1; Rare:72 | ||||
chr9:35714589-35714786 | Rare:56 | ||||
chr9:35723960-35724333 | Rare:91 | ||||
chr9:35724571-35724924 | Rare:79 | ||||
chr9:35741014-35741282 | Rare:60; Clinvar (benign):2 | ||||
chr9:35907832-35908029 | Common:1; Rare:28 | ||||
chr9:35909372-35909523 | Common:3; Rare:32 | ||||
chr9:35909882-35910227 | Common:1; Rare:79 | ||||
chr9:35918700-35918728 | Rare:2 | ||||
chr9:35929325-35929415 | Rare:15 | ||||
chr9:36220001-36220169 | Common:1; Rare:31; Clinvar:4 | ||||
chr9:37776229-37776232 |