Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:6632994-6633379 | Common:8; Rare:124; Clinvar:9; Clinvar (benign):4 | ||||
chr5:7868987-7869214 | Common:2; Rare:118; Clinvar (benign):1 | ||||
chr5:10249862-10250404 | Common:19; Rare:251; Clinvar:4; Clinvar (benign):2 | ||||
chr5:10353597-10353917 | Common:3; Rare:115 | ||||
chr5:16465276-16465913 | Rare:188 | ||||
chr5:16508640-16509149 | Common:5; Rare:89 | ||||
chr5:31532037-31532381 | Common:3; Rare:98 | ||||
chr5:32174277-32174444 | Common:2; Rare:60 | ||||
chr5:33440632-33441112 | Common:7; Rare:137 | ||||
chr5:34915472-34915750 | Common:1; Rare:70 | ||||
chr5:34929685-34930010 | Common:1; Rare:100 | ||||
chr5:36151816-36152153 | Rare:86 | ||||
chr5:36876650-36876938 | Common:1; Rare:85; Clinvar:1; Clinvar (benign):1 | ||||
chr5:36877102-36877175 | Rare:26 | ||||
chr5:37371053-37371359 | Common:2; Rare:73 |