Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr9:128724090-128724464 | Common:2; Rare:123 | ||||
chr9:128771854-128772024 | Rare:43 | ||||
chr9:128772450-128772499 | Rare:6 | ||||
chr9:128787091-128787354 | Common:4; Rare:85 | ||||
chr9:128881929-128882234 | Common:2; Rare:107 | ||||
chr9:128947549-128947722 | Common:1; Rare:80; Clinvar:5; Clinvar (benign):1 | ||||
chr9:129110650-129110960 | Common:4; Rare:70 | ||||
chr9:129141497-129141822 | Common:3; Rare:102 | ||||
chr9:129752993-129753174 | Rare:52 | ||||
chr9:129835208-129835499 | Common:3; Rare:115 | ||||
chr9:130043113-130043314 | Common:2; Rare:69 | ||||
chr9:130053847-130053983 | Common:1; Rare:57 | ||||
chr9:130579442-130579692 | Common:7; Rare:102 | ||||
chr9:130693594-130693794 | Rare:64 | ||||
chr9:131125446-131125637 | Common:1; Rare:89 |