Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:78056710-78057006 | Rare:65 | ||||
chr4:78372480-78372747 | Rare:58; Clinvar (pathogenic):1 | ||||
chr4:78629356-78629611 | Common:3; Rare:45 | ||||
chr4:79211513-79211681 | Common:1; Rare:32 | ||||
chr4:79412874-79413002 | Common:1; Rare:27 | ||||
chr4:84126185-84126360 | Common:2; Rare:46 | ||||
chr4:84965356-84965660 | Common:1; Rare:65 | ||||
chr4:87559601-87559768 | Common:1; Rare:24 | ||||
chr4:90128501-90128605 | Common:1; Rare:31 | ||||
chr4:90958585-90958617 | Common:1; Rare:2 | ||||
chr4:94039308-94039547 | Common:3; Rare:42 | ||||
chr4:94148101-94148253 | Rare:43 | ||||
chr4:95516459-95516619 | Common:4; Rare:34 | ||||
chr4:95547381-95547423 | Common:1; Rare:13 | ||||
chr4:103255692-103255930 | Common:8; Rare:76 |