Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr9:128921983-128922331 | Common:1; Rare:79 | ||||
chr9:128947531-128947722 | Common:1; Rare:85; Clinvar:5; Clinvar (benign):1 | ||||
chr9:129110628-129111029 | Common:5; Rare:123 | ||||
chr9:129835210-129835475 | Common:2; Rare:108 | ||||
chr9:130043100-130043324 | Common:2; Rare:77 | ||||
chr9:130053847-130053963 | Common:1; Rare:46 | ||||
chr9:130579445-130579692 | Common:7; Rare:101 | ||||
chr9:130713442-130713646 | Common:2; Rare:47 | ||||
chr9:131125407-131125642 | Common:2; Rare:107 | ||||
chr9:131502856-131503046 | Rare:71; Clinvar:3 | ||||
chr9:131531182-131531323 | Common:4; Rare:64 | ||||
chr9:132669924-132670046 | Common:1; Rare:58 | ||||
chr9:132878288-132878405 | Common:1; Rare:42 | ||||
chr9:132878818-132878946 | Rare:21 | ||||
chr9:133336146-133336503 | Common:2; Rare:133 |