Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:5823013-5823179 | Common:3; Rare:66 | ||||
chr7:12715686-12715974 | Common:1; Rare:52 | ||||
chr7:16644739-16644866 | Rare:39 | ||||
chr7:24979446-24979557 | Common:1; Rare:32 | ||||
chr7:26193252-26193673 | Rare:148; Clinvar (benign):2 | ||||
chr7:27168481-27168667 | Common:2; Rare:45 | ||||
chr7:32728742-32728853 | Common:4; Rare:37 | ||||
chr7:39733534-39733617 | Rare:16 | ||||
chr7:44019117-44019389 | Common:2; Rare:97 | ||||
chr7:44986592-44986756 | Common:2; Rare:84 | ||||
chr7:45768916-45769154 | Common:1; Rare:76 | ||||
chr7:53468208-53468328 | Common:2; Rare:27 | ||||
chr7:53811929-53812047 | Common:3; Rare:23 | ||||
chr7:55133817-55133969 | Common:1; Rare:31 | ||||
chr7:57579692-57579995 | Common:3; Rare:76 |