Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:112203771-112203807 | Rare:6 | ||||
chr7:112459141-112459387 | Common:1; Rare:46 | ||||
chr7:112462068-112462379 | Common:1; Rare:85 | ||||
chr7:112787172-112787324 | Common:1; Rare:23 | ||||
chr7:113118538-113118671 | Common:1; Rare:43 | ||||
chr7:114964854-114965172 | Common:1; Rare:59 | ||||
chr7:116465209-116465267 | Rare:7 | ||||
chr7:116465815-116466002 | Rare:23 | ||||
chr7:116502244-116502491 | Common:4; Rare:37 | ||||
chr7:116504964-116505288 | Rare:46 | ||||
chr7:116528474-116528734 | Rare:40 | ||||
chr7:116558676-116559014 | Common:3; Rare:64; Clinvar:1; Clinvar (benign):1 | ||||
chr7:116716105-116716388 | Common:1; Rare:58 | ||||
chr7:116757454-116757752 | Common:2; Rare:85; Clinvar:11; Clinvar (benign):7 | ||||
chr7:127584690-127584944 | Common:2; Rare:83 |