Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:152269533-152269696 | Rare:43 | ||||
chr3:155854374-155854743 | Rare:104 | ||||
chr3:156674353-156674618 | Common:3; Rare:77 | ||||
chr3:157160090-157160295 | Rare:87 | ||||
chr3:157543230-157543400 | Rare:38 | ||||
chr3:158105732-158105893 | Common:5; Rare:80; Clinvar:1; Clinvar (benign):1 | ||||
chr3:158110046-158110168 | Rare:26 | ||||
chr3:158644477-158644628 | Common:4; Rare:53; Clinvar (benign):5 | ||||
chr3:158801802-158802164 | Common:3; Rare:124 | ||||
chr3:160399196-160399307 | Rare:30; Clinvar:1 | ||||
chr3:160399518-160399658 | Rare:27 | ||||
chr3:160449748-160449894 | Common:1; Rare:45 | ||||
chr3:160565541-160565842 | Common:2; Rare:105 | ||||
chr3:161105311-161105395 | Common:1; Rare:34 | ||||
chr3:161221066-161221361 | Common:3; Rare:88 |