Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:122077481-122077744 | Common:1; Rare:115; Clinvar (benign):4 | ||||
chr5:122077970-122078668 | Common:1; Rare:152 | ||||
chr5:122845337-122845659 | Common:3; Rare:114 | ||||
chr5:123036645-123037002 | Common:2; Rare:89 | ||||
chr5:123511953-123512303 | Common:1; Rare:103 | ||||
chr5:126423347-126423613 | Rare:76 | ||||
chr5:127030511-127030760 | Common:2; Rare:60 | ||||
chr5:131162569-131162826 | Rare:61; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
chr5:131170704-131171006 | Common:1; Rare:62; Clinvar (benign):2 | ||||
chr5:131796928-131797215 | Rare:82 | ||||
chr5:132866457-132866676 | Common:1; Rare:69 | ||||
chr5:133051870-133052100 | Rare:87 | ||||
chr5:133968560-133968696 | Rare:65 | ||||
chr5:134004500-134004811 | Common:2; Rare:106 | ||||
chr5:134371026-134371152 | Common:1; Rare:33 |