Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:44112489-44112589 | Common:3; Rare:33 | ||||
chr7:44467542-44467881 | Common:3; Rare:65 | ||||
chr7:44986592-44986756 | Common:2; Rare:84 | ||||
chr7:45690455-45690637 | Common:1; Rare:42 | ||||
chr7:45768930-45769121 | Common:1; Rare:57 | ||||
chr7:45890256-45890738 | Common:1; Rare:125 | ||||
chr7:55031159-55031435 | Rare:47 | ||||
chr7:55181128-55181441 | Common:2; Rare:93; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
chr7:55182091-55182155 | Rare:10 | ||||
chr7:55188932-55189137 | Common:2; Rare:47 | ||||
chr7:65081233-65081403 | Common:2; Rare:55 | ||||
chr7:65750916-65751118 | Common:3; Rare:87 | ||||
chr7:65770719-65770935 | Common:6; Rare:69 | ||||
chr7:66493491-66493777 | Common:5; Rare:115 | ||||
chr7:66592345-66592437 | Common:1; Rare:34 |