Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:24114850-24115330 | Common:3; Rare:135 | ||||
chr14:24135943-24136299 | Common:1; Rare:114 | ||||
chr14:24136372-24136451 | Rare:21 | ||||
chr14:24141479-24141862 | Common:2; Rare:90 | ||||
chr14:24146543-24146761 | Rare:78 | ||||
chr14:24195316-24195364 | Rare:17 | ||||
chr14:24195391-24195781 | Common:2; Rare:93 | ||||
chr14:24213062-24213198 | Rare:27 | ||||
chr14:24213379-24213649 | Common:3; Rare:96 | ||||
chr14:24232295-24232515 | Common:8; Rare:57 | ||||
chr14:24232537-24232707 | Rare:41 | ||||
chr14:24232823-24232958 | Common:1; Rare:31 | ||||
chr14:24241673-24241993 | Rare:91; Clinvar:1; Clinvar (benign):1 | ||||
chr14:24242258-24242433 | Rare:58; Clinvar:1; Clinvar (benign):2 | ||||
chr14:24242560-24242774 | Common:1; Rare:53; Clinvar:1; Clinvar (benign):2 |