Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:169583592-169583804 | Common:6; Rare:67 | ||||
chr5:172188190-172188518 | Common:1; Rare:90 | ||||
chr5:176388993-176389192 | Rare:57 | ||||
chr5:177022622-177022744 | Rare:46 | ||||
chr5:177303651-177303988 | Common:4; Rare:139 | ||||
chr5:177351560-177351575 | Rare:2 | ||||
chr5:177447755-177448066 | Common:2; Rare:63 | ||||
chr5:178153663-178153694 | Rare:15; Clinvar:1 | ||||
chr5:179806895-179807066 | Common:3; Rare:60 | ||||
chr5:179823873-179824313 | Common:1; Rare:183; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr5:180810090-180810289 | Common:5; Rare:61 | ||||
chr5:181223500-181223710 | Common:3; Rare:54 | ||||
chr5:181261124-181261218 | Rare:25 | ||||
chr6:693054-693208 | Rare:49 | ||||
chr6:4021221-4021423 | Rare:94 |