Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:58460072-58460177 | Common:3; Rare:45 | ||||
chr5:59768487-59768549 | Rare:19 | ||||
chr5:60700129-60700264 | Common:3; Rare:42 | ||||
chr5:60945044-60945238 | Common:4; Rare:72; Clinvar:2; Clinvar (benign):4 | ||||
chr5:61162355-61162481 | Rare:22 | ||||
chr5:64768575-64768977 | Common:5; Rare:104 | ||||
chr5:65481849-65482032 | Common:1; Rare:33 | ||||
chr5:65563124-65563316 | Common:3; Rare:70 | ||||
chr5:65722076-65722347 | Common:4; Rare:93 | ||||
chr5:67004188-67004313 | Common:2; Rare:35 | ||||
chr5:69166927-69167182 | Common:1; Rare:60 | ||||
chr5:69369466-69370058 | Common:3; Rare:209 | ||||
chr5:69560044-69560263 | Common:2; Rare:58 | ||||
chr5:72955879-72956088 | Common:1; Rare:89 | ||||
chr5:73498371-73498556 | Common:1; Rare:57 |