Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:1801295-1801447 | Common:4; Rare:73; Clinvar:3; Clinvar (benign):1 | ||||
chr5:5422325-5422677 | Common:2; Rare:115 | ||||
chr5:6378485-6378699 | Rare:92 | ||||
chr5:7868991-7869204 | Common:2; Rare:109; Clinvar (benign):1 | ||||
chr5:10249859-10250225 | Common:17; Rare:164; Clinvar:1 | ||||
chr5:10353566-10353910 | Common:4; Rare:135 | ||||
chr5:16465442-16465899 | Rare:128 | ||||
chr5:31532032-31532362 | Common:3; Rare:96 | ||||
chr5:31854263-31854538 | Common:3; Rare:71 | ||||
chr5:32174254-32174389 | Common:1; Rare:53 | ||||
chr5:32531710-32531865 | Common:1; Rare:30 | ||||
chr5:33440624-33441101 | Common:7; Rare:133 | ||||
chr5:34656150-34656473 | Common:3; Rare:82 | ||||
chr5:34915471-34915753 | Common:1; Rare:73 | ||||
chr5:36151874-36152168 | Rare:89 |