Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr9:130053847-130053939 | Common:1; Rare:30 | ||||
chr9:130579446-130579692 | Common:6; Rare:101 | ||||
chr9:130693594-130693789 | Rare:63 | ||||
chr9:131096239-131096541 | Common:3; Rare:77 | ||||
chr9:131125407-131125637 | Common:2; Rare:105 | ||||
chr9:131502866-131503033 | Rare:58; Clinvar:3 | ||||
chr9:131531170-131531340 | Common:9; Rare:78 | ||||
chr9:132354922-132355252 | Common:4; Rare:109 | ||||
chr9:132669939-132670040 | Common:1; Rare:49 | ||||
chr9:132670330-132670506 | Rare:57 | ||||
chr9:132878279-132878361 | Common:1; Rare:28 | ||||
chr9:133061730-133062141 | Common:1; Rare:72; Clinvar (benign):1 | ||||
chr9:133348045-133348268 | Common:2; Rare:92 | ||||
chr9:133356449-133356606 | Common:1; Rare:72; Clinvar (benign):2 | ||||
chr9:133376003-133376370 | Common:1; Rare:132 |