Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:143001378-143001631 | Common:4; Rare:89 | ||||
chr3:149377644-149377812 | Common:1; Rare:41 | ||||
chr3:149813010-149813265 | Common:2; Rare:86 | ||||
chr3:150603139-150603347 | Common:2; Rare:77 | ||||
chr3:152268542-152268983 | Common:2; Rare:171 | ||||
chr3:152269054-152269332 | Rare:79 | ||||
chr3:152269533-152269696 | Rare:43 | ||||
chr3:152834788-152835100 | Common:1; Rare:80 | ||||
chr3:154121264-154121451 | Common:2; Rare:80 | ||||
chr3:155854350-155854748 | Rare:109 | ||||
chr3:156674357-156674653 | Common:3; Rare:88 | ||||
chr3:157160018-157160295 | Rare:115 | ||||
chr3:158105732-158105878 | Common:5; Rare:74; Clinvar:1; Clinvar (benign):1 | ||||
chr3:158672607-158672624 | Rare:4 | ||||
chr3:158801967-158802155 | Common:2; Rare:88 |