Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:110449511-110449721 | Common:3; Rare:56; Clinvar:1; Clinvar (benign):1 | ||||
chr14:24254023-24254074 | Rare:8 | ||||
chr14:24258260-24258563 | Rare:71; Clinvar:2; Clinvar (pathogenic):3 | ||||
chr14:31103039-31103240 | Common:1; Rare:39 | ||||
chr14:32203267-32203642 | Common:13; Rare:159 | ||||
chr14:35402158-35402673 | Common:4; Rare:146; Clinvar:3; Clinvar (benign):2 | ||||
chr14:49633956-49634064 | Common:1; Rare:43; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr14:49862639-49863044 | Common:1; Rare:185 | ||||
chr14:50009051-50009246 | Rare:32 | ||||
chr14:51512127-51512447 | Common:2; Rare:57 | ||||
chr14:51515639-51515865 | Common:3; Rare:37 | ||||
chr14:51564148-51564380 | Common:2; Rare:30 | ||||
chr14:51599911-51600248 | Common:1; Rare:66 | ||||
chr14:52001702-52001805 | Rare:22 | ||||
chr14:58266085-58266187 | Common:1; Rare:22 |