Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:178130887-178131039 | Rare:40 | ||||
chr5:178153788-178154181 | Rare:109; Clinvar:5; Clinvar (benign):1 | ||||
chr5:178204339-178204534 | Common:3; Rare:68 | ||||
chr5:178232340-178232471 | Common:5; Rare:73 | ||||
chr5:178232784-178232908 | Common:1; Rare:56 | ||||
chr5:178626559-178626659 | Common:1; Rare:28 | ||||
chr5:178626949-178627239 | Common:7; Rare:97 | ||||
chr5:178859800-178860043 | Common:2; Rare:73 | ||||
chr5:178940963-178941239 | Common:1; Rare:73 | ||||
chr5:179023679-179023889 | Common:2; Rare:71 | ||||
chr5:179060236-179060432 | Common:1; Rare:55 | ||||
chr5:179550528-179550561 | Common:2; Rare:4 | ||||
chr5:179550797-179550858 | Rare:22 | ||||
chr5:179559530-179559809 | Common:1; Rare:80 | ||||
chr5:179623046-179623452 | Common:3; Rare:154 |