Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:79279534-79279732 | Common:1; Rare:42 | ||||
chr14:81220855-81221054 | Common:1; Rare:95 | ||||
chr14:81221275-81221471 | Common:1; Rare:49 | ||||
chr14:85530024-85530191 | Common:1; Rare:36 | ||||
chr14:88824345-88824716 | Common:2; Rare:106; Clinvar:3; Clinvar (benign):1 | ||||
chr14:90396991-90397237 | Common:5; Rare:119; Clinvar (benign):2 | ||||
chr14:91060142-91060393 | Common:3; Rare:93 | ||||
chr14:91114288-91114402 | Rare:18 | ||||
chr14:91510242-91510627 | Common:1; Rare:122 | ||||
chr14:91836421-91836681 | Common:12; Rare:44 | ||||
chr14:92040004-92040192 | Common:3; Rare:58; Clinvar:3; Clinvar (benign):2 | ||||
chr14:92121647-92122003 | Common:5; Rare:122 | ||||
chr14:92748552-92748788 | Rare:62 | ||||
chr14:92793988-92794418 | Rare:137 | ||||
chr14:93115770-93115995 | Common:1; Rare:65 |