Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr9:34049186-34049267 | Common:1; Rare:19 | ||||
chr9:34126622-34126786 | Rare:54 | ||||
chr9:34178952-34179061 | Common:1; Rare:29 | ||||
chr9:34329213-34329620 | Common:1; Rare:125 | ||||
chr9:34612082-34612223 | Common:8; Rare:47 | ||||
chr9:34637725-34637924 | Rare:60 | ||||
chr9:34651989-34652207 | Rare:67 | ||||
chr9:34665381-34665660 | Rare:91 | ||||
chr9:35079996-35080172 | Common:3; Rare:48; Clinvar:2; Clinvar (benign):2 | ||||
chr9:35489960-35490085 | Rare:28 | ||||
chr9:35657865-35657968 | Common:1; Rare:118; Clinvar:18; Clinvar (benign):3; Clinvar (pathogenic):6 | ||||
chr9:35657970-35658397 | Common:7; Rare:317; Clinvar:20; Clinvar (benign):11; Clinvar (pathogenic):34 | ||||
chr9:35732073-35732320 | Common:1; Rare:66 | ||||
chr9:35732365-35732676 | Common:2; Rare:79 | ||||
chr9:35749001-35749331 | Common:2; Rare:119 |