Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:131170715-131171006 | Common:1; Rare:58; Clinvar (benign):2 | ||||
chr5:131263908-131264133 | Rare:82 | ||||
chr5:131635146-131635393 | Common:1; Rare:95 | ||||
chr5:131796936-131797215 | Rare:80 | ||||
chr5:132369623-132369759 | Common:2; Rare:39 | ||||
chr5:132410603-132411017 | Common:1; Rare:86 | ||||
chr5:132490774-132491020 | Rare:64 | ||||
chr5:132557084-132557232 | Rare:46 | ||||
chr5:132866457-132866688 | Common:1; Rare:74; Clinvar:1; Clinvar (benign):1 | ||||
chr5:132963286-132963393 | Rare:22 | ||||
chr5:132963503-132963782 | Rare:70 | ||||
chr5:133051862-133052295 | Common:1; Rare:144 | ||||
chr5:133968570-133968688 | Rare:55 | ||||
chr5:134004510-134004860 | Common:2; Rare:121 | ||||
chr5:134004935-134005030 | Rare:21 |