Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:77707877-77708108 | Rare:104 | ||||
chr14:77761109-77761223 | Rare:48 | ||||
chr14:81220875-81221163 | Common:1; Rare:131 | ||||
chr14:88005075-88005192 | Rare:15 | ||||
chr14:89955627-89955987 | Common:10; Rare:103; Clinvar:3; Clinvar (benign):1 | ||||
chr14:90403820-90403905 | Rare:20 | ||||
chr14:91060577-91060694 | Rare:40 | ||||
chr14:91416861-91416900 | Rare:14 | ||||
chr14:91417671-91417977 | Common:4; Rare:103 | ||||
chr14:91510254-91510644 | Common:1; Rare:129 | ||||
chr14:92040052-92040192 | Common:1; Rare:36 | ||||
chr14:92121665-92121949 | Common:4; Rare:95 | ||||
chr14:92794004-92794395 | Rare:127 | ||||
chr14:93184834-93185020 | Rare:65 | ||||
chr14:93207125-93207298 | Common:2; Rare:82 |