Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:37371053-37371245 | Rare:60 | ||||
chr5:38845761-38846058 | Common:1; Rare:77 | ||||
chr5:43603072-43603219 | Rare:38 | ||||
chr5:44808768-44808966 | Common:2; Rare:61 | ||||
chr5:50667357-50667421 | Common:1; Rare:19 | ||||
chr5:50667754-50667857 | Common:1; Rare:32 | ||||
chr5:53109719-53109915 | Common:1; Rare:103; Clinvar:3 | ||||
chr5:55307624-55308010 | Common:4; Rare:129 | ||||
chr5:56952110-56952403 | Rare:109 | ||||
chr5:57173785-57174168 | Common:1; Rare:127 | ||||
chr5:59039529-59039657 | Common:1; Rare:26 | ||||
chr5:60488061-60488302 | Rare:42 | ||||
chr5:60700092-60700224 | Common:1; Rare:52 | ||||
chr5:60945006-60945372 | Common:6; Rare:149; Clinvar:7; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
chr5:61162251-61162498 | Common:1; Rare:51 |