Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:47940477-47940772 | Common:1; Rare:57 | ||||
chr7:48140166-48140368 | Rare:32 | ||||
chr7:55019994-55020199 | Rare:46 | ||||
chr7:55067029-55067158 | Common:2; Rare:28 | ||||
chr7:55508846-55508958 | Rare:19 | ||||
chr7:65081203-65081417 | Common:3; Rare:73 | ||||
chr7:65750910-65751133 | Common:3; Rare:100 | ||||
chr7:65770719-65770936 | Common:6; Rare:69 | ||||
chr7:66086438-66086645 | Rare:51; Clinvar:3; Clinvar (pathogenic):1 | ||||
chr7:66493507-66493741 | Common:4; Rare:98 | ||||
chr7:66554353-66554427 | Common:3; Rare:13 | ||||
chr7:66592287-66592454 | Common:2; Rare:62 | ||||
chr7:66654461-66654578 | Rare:44 | ||||
chr7:66844872-66845087 | Common:2; Rare:88 | ||||
chr7:67302396-67302737 | Common:5; Rare:109 |