Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:179023676-179023832 | Common:2; Rare:44 | ||||
chr5:179559559-179559819 | Common:1; Rare:76 | ||||
chr5:179698382-179698422 | Common:1; Rare:13 | ||||
chr5:179698634-179699092 | Common:4; Rare:158 | ||||
chr5:179806304-179806458 | Rare:50 | ||||
chr5:179806591-179806727 | Common:1; Rare:39 | ||||
chr5:179806879-179807107 | Common:3; Rare:82 | ||||
chr5:179820776-179820907 | Common:2; Rare:48; Clinvar (benign):1 | ||||
chr5:179858797-179858958 | Rare:91 | ||||
chr5:179907811-179908009 | Common:2; Rare:98 | ||||
chr5:180072128-180072225 | Common:1; Rare:42 | ||||
chr5:180810081-180810223 | Common:2; Rare:36 | ||||
chr5:180861150-180861394 | Common:2; Rare:98 | ||||
chr5:181223118-181223328 | Rare:75 | ||||
chr5:181223653-181223768 | Common:3; Rare:28 |