Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:25941011-25941208 | Common:1; Rare:31 | ||||
chr7:26193313-26193695 | Rare:139; Clinvar (benign):2 | ||||
chr7:32942514-32942645 | Common:1; Rare:39 | ||||
chr7:42888727-42888953 | Common:1; Rare:46 | ||||
chr7:43990105-43990186 | Rare:14 | ||||
chr7:43990192-43990563 | Common:1; Rare:77 | ||||
chr7:44019132-44019389 | Common:2; Rare:86 | ||||
chr7:44986597-44986739 | Common:2; Rare:72 | ||||
chr7:45768930-45769158 | Common:2; Rare:72 | ||||
chr7:54831761-54831820 | Rare:8 | ||||
chr7:65750916-65751080 | Common:2; Rare:66 | ||||
chr7:66493507-66493762 | Common:4; Rare:107 | ||||
chr7:66654214-66654567 | Common:2; Rare:119 | ||||
chr7:67302400-67302742 | Common:5; Rare:110 | ||||
chr7:73005872-73006159 | Rare:24 |