Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr9:6015608-6015686 | Rare:35 | ||||
chr9:6757865-6758108 | Common:5; Rare:94 | ||||
chr9:15422641-15422880 | Common:1; Rare:100 | ||||
chr9:19049328-19049423 | Rare:39 | ||||
chr9:19102885-19103084 | Common:2; Rare:85 | ||||
chr9:19127437-19127568 | Common:2; Rare:35 | ||||
chr9:19230366-19230825 | Common:7; Rare:201 | ||||
chr9:19380191-19380360 | Common:4; Rare:84 | ||||
chr9:19408782-19409012 | Common:3; Rare:91 | ||||
chr9:21335369-21335476 | Common:2; Rare:38 | ||||
chr9:26892426-26892503 | Rare:38 | ||||
chr9:26947132-26947245 | Rare:40 | ||||
chr9:26956302-26956459 | Common:2; Rare:57 | ||||
chr9:27573430-27573526 | Common:5; Rare:50 | ||||
chr9:33001570-33001721 | Common:2; Rare:80; Clinvar (benign):3 |