Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:82429269-82429631 | Common:2; Rare:206; Clinvar:12; Clinvar (benign):7 | ||||
chr4:82429977-82430073 | Rare:28 | ||||
chr4:82430407-82430860 | Common:3; Rare:160 | ||||
chr4:82900466-82900714 | Rare:71 | ||||
chr4:83455843-83456068 | Common:1; Rare:85 | ||||
chr4:88158610-88158718 | Rare:33 | ||||
chr4:88523698-88523855 | Common:2; Rare:55 | ||||
chr4:89111349-89111641 | Common:4; Rare:104 | ||||
chr4:98261155-98261499 | Common:1; Rare:106 | ||||
chr4:98929115-98929327 | Common:3; Rare:56 | ||||
chr4:99088702-99088891 | Common:6; Rare:84 | ||||
chr4:99950269-99950523 | Rare:51 | ||||
chr4:101347444-101347786 | Common:4; Rare:98 | ||||
chr4:102826748-102826914 | Rare:42 | ||||
chr4:102827041-102827390 | Common:4; Rare:128 |