Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr9:131502883-131503030 | Rare:50; Clinvar:3 | ||||
chr9:131531188-131531363 | Common:9; Rare:79 | ||||
chr9:132354932-132355298 | Common:5; Rare:117 | ||||
chr9:132406801-132406903 | Rare:34 | ||||
chr9:132669937-132670046 | Common:1; Rare:53 | ||||
chr9:132670173-132670500 | Rare:107 | ||||
chr9:132878272-132878403 | Common:1; Rare:50 | ||||
chr9:133030447-133030743 | Common:4; Rare:79 | ||||
chr9:133163903-133164039 | Common:3; Rare:33 | ||||
chr9:133336133-133336283 | Common:1; Rare:57 | ||||
chr9:133348039-133348253 | Common:2; Rare:80 | ||||
chr9:133356464-133356628 | Common:1; Rare:75; Clinvar (benign):2 | ||||
chr9:133375965-133376366 | Common:3; Rare:146 | ||||
chr9:133459946-133460058 | Common:1; Rare:49 | ||||
chr9:134641551-134641771 | Common:1; Rare:64 |