Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:77075967-77076057 | Rare:50 | ||||
chr4:77862659-77862863 | Common:3; Rare:71 | ||||
chr4:78551651-78551842 | Rare:50 | ||||
chr4:82891107-82891317 | Common:1; Rare:82 | ||||
chr4:82900526-82900691 | Rare:49 | ||||
chr4:83455814-83456072 | Common:2; Rare:100 | ||||
chr4:89111371-89111569 | Common:3; Rare:72 | ||||
chr4:94451745-94451982 | Common:3; Rare:79 | ||||
chr4:99088697-99088884 | Common:6; Rare:83 | ||||
chr4:99563989-99564127 | Common:2; Rare:45; Clinvar:1; Clinvar (benign):2 | ||||
chr4:102827470-102827662 | Common:1; Rare:73 | ||||
chr4:102827668-102828291 | Common:6; Rare:197 | ||||
chr4:102868873-102869061 | Common:2; Rare:60 | ||||
chr4:105708649-105708791 | Rare:40 | ||||
chr4:106316196-106316588 | Common:5; Rare:126 |