Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:59464185-59464307 | Common:1; Rare:61 | ||||
chr14:60637117-60637321 | Common:1; Rare:46 | ||||
chr14:61586200-61586255 | Common:2; Rare:14 | ||||
chr14:61751089-61751223 | Rare:34 | ||||
chr14:61864463-61864565 | Rare:20 | ||||
chr14:61864737-61864895 | Common:1; Rare:34 | ||||
chr14:62117192-62117439 | Common:2; Rare:45 | ||||
chr14:63178137-63178308 | Rare:28 | ||||
chr14:63497004-63497058 | Rare:9 | ||||
chr14:63542313-63542398 | Rare:19 | ||||
chr14:64113154-64113382 | Common:1; Rare:62; Clinvar (benign):3 | ||||
chr14:64220262-64220499 | Rare:70; Clinvar:2 | ||||
chr14:64379316-64379416 | Rare:15 | ||||
chr14:64430152-64430229 | Rare:21 | ||||
chr14:64539594-64539639 | Common:1; Rare:9 |