Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:14145938-14146223 | Rare:40 | ||||
chr5:32173359-32173415 | Rare:8 | ||||
chr5:42950725-42951001 | Rare:74 | ||||
chr5:43034438-43034693 | Common:1; Rare:50 | ||||
chr5:43034778-43034877 | Rare:15 | ||||
chr5:43041440-43041632 | Common:2; Rare:33 | ||||
chr5:43041725-43041849 | Rare:22 | ||||
chr5:61391896-61391953 | Rare:10 | ||||
chr5:65925542-65925835 | Rare:115 | ||||
chr5:66003274-66003487 | Common:1; Rare:44 | ||||
chr5:78175694-78175819 | Common:2; Rare:37; Clinvar (benign):1 | ||||
chr5:87390471-87390758 | Rare:72 | ||||
chr5:93554902-93554937 | Rare:5 | ||||
chr5:94568896-94569041 | Rare:23 | ||||
chr5:100051602-100051906 | Common:2; Rare:58 |