Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:74019252-74019432 | Common:1; Rare:71 | ||||
chr14:74493266-74493770 | Common:4; Rare:160; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr14:74713077-74713200 | Rare:61 | ||||
chr14:74881778-74881961 | Common:1; Rare:80 | ||||
chr14:75002741-75002952 | Common:1; Rare:60; Clinvar:2 | ||||
chr14:75069488-75069727 | Common:1; Rare:56 | ||||
chr14:75127001-75127128 | Rare:42 | ||||
chr14:75147669-75148006 | Common:3; Rare:55 | ||||
chr14:75280366-75280681 | Common:2; Rare:73 | ||||
chr14:75660819-75661212 | Common:2; Rare:90 | ||||
chr14:75661223-75661326 | Common:2; Rare:27 | ||||
chr14:77320838-77321051 | Rare:64; Clinvar:1 | ||||
chr14:77377053-77377415 | Common:2; Rare:106 | ||||
chr14:77457556-77457845 | Common:1; Rare:89 | ||||
chr14:77707991-77708114 | Rare:59 |