Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:77199794-77199862 | Rare:21 | ||||
chr7:77696221-77696503 | Rare:123 | ||||
chr7:77798360-77798956 | Common:1; Rare:144 | ||||
chr7:79453835-79454093 | Common:1; Rare:64 | ||||
chr7:80134696-80135040 | Common:2; Rare:110 | ||||
chr7:87152379-87152655 | Common:2; Rare:84 | ||||
chr7:87345443-87345730 | Common:5; Rare:90 | ||||
chr7:87876255-87876641 | Common:2; Rare:174 | ||||
chr7:90211633-90211890 | Common:3; Rare:78 | ||||
chr7:90346586-90346752 | Common:4; Rare:73 | ||||
chr7:91880677-91880815 | Common:1; Rare:37 | ||||
chr7:92245857-92245974 | Rare:33; Clinvar:3; Clinvar (benign):1 | ||||
chr7:92528389-92528807 | Common:3; Rare:129; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
chr7:92833925-92834074 | Rare:37 | ||||
chr7:93232191-93232401 | Common:2; Rare:40 |