Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:177467040-177467333 | Common:1; Rare:88 | ||||
chr5:177497529-177497865 | Common:1; Rare:123 | ||||
chr5:177509828-177509927 | Rare:42 | ||||
chr5:177516932-177517093 | Rare:56; Clinvar (pathogenic):1 | ||||
chr5:178130882-178131039 | Rare:42 | ||||
chr5:178153758-178154110 | Rare:110; Clinvar:5; Clinvar (benign):1 | ||||
chr5:178232380-178232610 | Common:6; Rare:115 | ||||
chr5:178859813-178860114 | Common:4; Rare:87 | ||||
chr5:178940943-178941239 | Common:1; Rare:78 | ||||
chr5:179550475-179550858 | Common:3; Rare:173 | ||||
chr5:179559559-179559793 | Common:1; Rare:67 | ||||
chr5:179623602-179623954 | Common:4; Rare:128 | ||||
chr5:179698580-179699099 | Common:4; Rare:184 | ||||
chr5:179806278-179806404 | Rare:33 | ||||
chr5:179806910-179807063 | Common:2; Rare:51 |