Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:236395143-236395286 | Rare:34 | ||||
chr1:236395330-236395513 | Rare:45 | ||||
chr1:236395807-236395966 | Common:1; Rare:39 | ||||
chr1:236523309-236523614 | Common:2; Rare:68 | ||||
chr1:236523759-236523816 | Common:1; Rare:10 | ||||
chr1:236523818-236524064 | Common:3; Rare:64 | ||||
chr1:236524213-236524236 | Rare:11 | ||||
chr1:236524401-236524656 | Common:2; Rare:66 | ||||
chr1:236604408-236604691 | Common:5; Rare:87 | ||||
chr1:236794984-236795500 | Common:6; Rare:195; Clinvar:4 | ||||
chr1:236795620-236795914 | Common:3; Rare:118; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr1:236795918-236796142 | Common:1; Rare:55 | ||||
chr1:239386423-239386691 | Common:1; Rare:39 | ||||
chr1:241519220-241519308 | Rare:15 | ||||
chr1:241519451-241519542 | Common:1; Rare:26 |