Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:88523699-88523893 | Common:3; Rare:61 | ||||
chr4:88592306-88592533 | Common:1; Rare:68 | ||||
chr4:88823148-88823410 | Common:2; Rare:48 | ||||
chr4:94451769-94451982 | Common:3; Rare:73 | ||||
chr4:95549203-95549381 | Common:1; Rare:31 | ||||
chr4:98143484-98143642 | Common:1; Rare:39 | ||||
chr4:98261113-98261499 | Common:3; Rare:128 | ||||
chr4:98657647-98657803 | Rare:34 | ||||
chr4:98658609-98658905 | Common:2; Rare:79 | ||||
chr4:98929101-98929358 | Common:3; Rare:65 | ||||
chr4:98995518-98995748 | Common:5; Rare:79 | ||||
chr4:99088696-99088884 | Common:6; Rare:85 | ||||
chr4:99563989-99564122 | Common:2; Rare:42; Clinvar (benign):2 | ||||
chr4:99894357-99894608 | Common:2; Rare:89 | ||||
chr4:99950239-99950535 | Rare:67 |