Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:73950056-73950351 | Common:6; Rare:136; Clinvar (benign):4 | ||||
chr14:74019212-74019436 | Common:2; Rare:90 | ||||
chr14:74084397-74084755 | Common:7; Rare:91 | ||||
chr14:74493210-74493777 | Common:4; Rare:185; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
chr14:74612227-74612435 | Rare:37 | ||||
chr14:74713050-74713218 | Rare:96 | ||||
chr14:74948521-74948670 | Common:2; Rare:45 | ||||
chr14:75002734-75002982 | Common:1; Rare:81; Clinvar:2 | ||||
chr14:75069503-75069681 | Common:1; Rare:40 | ||||
chr14:75126985-75127120 | Rare:47 | ||||
chr14:75127343-75127374 | Rare:8 | ||||
chr14:75176353-75176675 | Rare:98 | ||||
chr14:75427653-75427749 | Rare:21 | ||||
chr14:75660789-75661520 | Common:7; Rare:191 | ||||
chr14:76151785-76151984 | Rare:67 |