Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:58460043-58460192 | Common:4; Rare:63 | ||||
chr5:60488066-60488214 | Rare:22 | ||||
chr5:60945046-60945235 | Common:4; Rare:69; Clinvar:2; Clinvar (benign):4 | ||||
chr5:61162215-61162499 | Common:1; Rare:58 | ||||
chr5:62403842-62404033 | Common:3; Rare:66 | ||||
chr5:64768575-64768946 | Common:5; Rare:98 | ||||
chr5:65563116-65563406 | Common:3; Rare:115 | ||||
chr5:65722057-65722380 | Common:4; Rare:108 | ||||
chr5:66144059-66144351 | Common:3; Rare:105 | ||||
chr5:67004051-67004297 | Common:3; Rare:89 | ||||
chr5:67004543-67004701 | Common:1; Rare:43 | ||||
chr5:69166927-69167199 | Common:2; Rare:64 | ||||
chr5:69369473-69369865 | Common:1; Rare:157 | ||||
chr5:69492461-69492832 | Common:1; Rare:107; Clinvar (benign):3 | ||||
chr5:72107202-72107490 | Common:2; Rare:118 |