Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:31208110-31208212 | Common:2; Rare:24 | ||||
chr14:31420511-31420752 | Common:3; Rare:77 | ||||
chr14:31561088-31561481 | Common:4; Rare:109; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr14:32076128-32076326 | Rare:58 | ||||
chr14:32076631-32077041 | Common:3; Rare:122 | ||||
chr14:33951058-33951229 | Common:1; Rare:58 | ||||
chr14:34018736-34018887 | Common:1; Rare:25 | ||||
chr14:34462200-34462558 | Common:1; Rare:128 | ||||
chr14:34539619-34539875 | Common:1; Rare:73 | ||||
chr14:34629925-34630246 | Common:5; Rare:125 | ||||
chr14:34713490-34713803 | Common:1; Rare:90; Clinvar:2; Clinvar (benign):2 | ||||
chr14:34714538-34714793 | Common:4; Rare:94 | ||||
chr14:34874765-34875040 | Common:3; Rare:82 | ||||
chr14:34875155-34875404 | Rare:94 | ||||
chr14:34982373-34982709 | Common:1; Rare:136 |