Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:5455945-5456171 | Common:2; Rare:49 | ||||
chr7:16420571-16420795 | Common:2; Rare:57 | ||||
chr7:26101469-26101657 | Common:2; Rare:25 | ||||
chr7:26193512-26193714 | Rare:70; Clinvar (benign):2 | ||||
chr7:26198064-26198274 | Common:1; Rare:74 | ||||
chr7:26198846-26199168 | Rare:148 | ||||
chr7:26199283-26199568 | Common:2; Rare:115 | ||||
chr7:26398818-26398957 | Common:2; Rare:37 | ||||
chr7:27168385-27168720 | Common:3; Rare:71 | ||||
chr7:29647532-29647887 | Common:6; Rare:62 | ||||
chr7:29684910-29685017 | Rare:39 | ||||
chr7:30574765-30574816 | Rare:5 | ||||
chr7:32727939-32728139 | Common:1; Rare:66 | ||||
chr7:32728603-32728849 | Common:7; Rare:79 | ||||
chr7:32942514-32942697 | Common:2; Rare:56 |