Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr9:131125446-131125651 | Common:1; Rare:99 | ||||
chr9:131531182-131531345 | Common:9; Rare:74 | ||||
chr9:132669937-132670078 | Common:1; Rare:64 | ||||
chr9:132670173-132670518 | Rare:116 | ||||
chr9:132878272-132878381 | Common:1; Rare:40 | ||||
chr9:132878847-132878985 | Rare:23 | ||||
chr9:133030471-133030743 | Common:4; Rare:70 | ||||
chr9:133348039-133348247 | Common:2; Rare:77 | ||||
chr9:133356452-133356630 | Common:1; Rare:84; Clinvar (benign):2 | ||||
chr9:133376015-133376346 | Common:1; Rare:120 | ||||
chr9:133417963-133418094 | Common:1; Rare:33 | ||||
chr9:134371845-134371962 | Rare:31 | ||||
chr9:136410609-136410686 | Rare:40 | ||||
chr9:136807797-136808097 | Common:2; Rare:114 | ||||
chr9:136886249-136886533 | Common:2; Rare:83 |