Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:49693194-49693349 | Rare:65 | ||||
chr14:49693360-49693523 | Common:1; Rare:58 | ||||
chr14:49767311-49767452 | Rare:21 | ||||
chr14:49767495-49767772 | Common:2; Rare:94 | ||||
chr14:49767904-49768236 | Common:3; Rare:120 | ||||
chr14:49768529-49768663 | Rare:46 | ||||
chr14:49852569-49853193 | Common:5; Rare:177 | ||||
chr14:49892353-49892713 | Common:5; Rare:95 | ||||
chr14:49892769-49893211 | Common:2; Rare:175 | ||||
chr14:49893346-49893625 | Common:4; Rare:87 | ||||
chr14:50116453-50116786 | Common:1; Rare:159 | ||||
chr14:50231146-50231260 | Common:1; Rare:48; Clinvar (benign):1 | ||||
chr14:50231513-50232082 | Common:2; Rare:192 | ||||
chr14:50311890-50312427 | Common:3; Rare:216; Clinvar:3; Clinvar (benign):3 | ||||
chr14:50312505-50312871 | Common:8; Rare:110 |