Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:175968182-175968331 | Common:1; Rare:38 | ||||
chr5:176361666-176361896 | Common:1; Rare:64 | ||||
chr5:176388476-176388847 | Common:4; Rare:144 | ||||
chr5:176389035-176389356 | Common:2; Rare:95 | ||||
chr5:177006680-177006965 | Common:2; Rare:89 | ||||
chr5:177022622-177022746 | Rare:46 | ||||
chr5:177133226-177133258 | Rare:5 | ||||
chr5:177133438-177133853 | Rare:149 | ||||
chr5:177303683-177304020 | Common:3; Rare:133 | ||||
chr5:177497545-177497865 | Common:1; Rare:118 | ||||
chr5:177516932-177517068 | Rare:48; Clinvar (pathogenic):1 | ||||
chr5:177592083-177592224 | Common:1; Rare:54 | ||||
chr5:178130878-178131039 | Rare:43 | ||||
chr5:178232555-178232908 | Common:4; Rare:118 | ||||
chr5:179023679-179023838 | Common:2; Rare:47 |