Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:38459315-38459465 | Rare:37 | ||||
chr3:39384246-39384457 | Common:7; Rare:49 | ||||
chr3:39411692-39412000 | Rare:76 | ||||
chr3:40453163-40453435 | Common:6; Rare:61 | ||||
chr3:41225331-41225785 | Rare:95; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr3:41227052-41227352 | Rare:64; Clinvar (pathogenic):1 | ||||
chr3:41237807-41238055 | Common:1; Rare:66 | ||||
chr3:41681589-41681819 | Common:2; Rare:78; Clinvar (benign):1 | ||||
chr3:42632350-42632620 | Common:2; Rare:58 | ||||
chr3:42654377-42654635 | Rare:76 | ||||
chr3:42770535-42770600 | Rare:15 | ||||
chr3:43490703-43491128 | Rare:84 | ||||
chr3:43998832-43998898 | Rare:18 | ||||
chr3:43999083-43999509 | Rare:118 | ||||
chr3:44023174-44023368 | Common:1; Rare:36 |