Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:24232754-24232958 | Common:1; Rare:48 | ||||
chr14:24242247-24242413 | Common:1; Rare:55; Clinvar:1; Clinvar (benign):2 | ||||
chr14:24242562-24242769 | Common:1; Rare:49; Clinvar:1; Clinvar (benign):2 | ||||
chr14:24299726-24299877 | Common:4; Rare:44 | ||||
chr14:24367911-24368209 | Common:2; Rare:49 | ||||
chr14:24429855-24429965 | Rare:25 | ||||
chr14:24442666-24443043 | Common:5; Rare:117 | ||||
chr14:30622190-30622344 | Rare:55 | ||||
chr14:31025635-31025675 | Rare:12 | ||||
chr14:31420526-31420763 | Common:3; Rare:71 | ||||
chr14:32076657-32077043 | Common:3; Rare:115 | ||||
chr14:34462204-34462577 | Common:1; Rare:132 | ||||
chr14:34539619-34539896 | Common:1; Rare:77 | ||||
chr14:34875271-34875459 | Rare:74 | ||||
chr14:34982372-34982709 | Common:1; Rare:136 |