Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:87391148-87391347 | Common:1; Rare:71 | ||||
chr4:87422507-87422647 | Common:1; Rare:39 | ||||
chr4:88158612-88158752 | Rare:37 | ||||
chr4:88378781-88379082 | Common:3; Rare:96 | ||||
chr4:88523689-88523835 | Common:2; Rare:53 | ||||
chr4:88592305-88592542 | Common:1; Rare:74 | ||||
chr4:89111371-89111588 | Common:3; Rare:85 | ||||
chr4:94451747-94451993 | Common:3; Rare:83 | ||||
chr4:98261167-98261519 | Common:1; Rare:113 | ||||
chr4:98658609-98658828 | Common:2; Rare:64 | ||||
chr4:98929101-98929397 | Common:3; Rare:72 | ||||
chr4:99088696-99088879 | Common:6; Rare:83 | ||||
chr4:99563921-99564158 | Common:2; Rare:77; Clinvar:2; Clinvar (benign):2 | ||||
chr4:99950212-99950528 | Common:1; Rare:79 | ||||
chr4:101347519-101347834 | Common:5; Rare:97 |