Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:87876324-87876634 | Common:2; Rare:133 | ||||
chr7:88220013-88220129 | Rare:60 | ||||
chr7:88306873-88307173 | Rare:62 | ||||
chr7:90211628-90211913 | Common:4; Rare:87 | ||||
chr7:90245101-90245253 | Common:1; Rare:53 | ||||
chr7:90346602-90346736 | Common:3; Rare:58 | ||||
chr7:90403312-90403539 | Common:1; Rare:57 | ||||
chr7:90595855-90596031 | Common:6; Rare:62 | ||||
chr7:91880677-91880816 | Common:1; Rare:37 | ||||
chr7:92134409-92134603 | Rare:61 | ||||
chr7:92134717-92134923 | Common:3; Rare:61 | ||||
chr7:92245886-92245979 | Rare:28; Clinvar:3; Clinvar (benign):1 | ||||
chr7:92528392-92528808 | Common:3; Rare:130; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
chr7:92833902-92834089 | Rare:46 | ||||
chr7:93232189-93232431 | Common:3; Rare:54 |