Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr9:127899507-127899749 | Rare:85 | ||||
chr9:128275910-128276307 | Common:5; Rare:173 | ||||
chr9:128322408-128322535 | Common:1; Rare:44 | ||||
chr9:128322739-128322861 | Common:2; Rare:46; Clinvar (benign):5 | ||||
chr9:128371224-128371389 | Rare:57 | ||||
chr9:128552408-128552597 | Rare:73; Clinvar:1 | ||||
chr9:128724102-128724464 | Common:2; Rare:116 | ||||
chr9:128881929-128882202 | Common:2; Rare:93 | ||||
chr9:128921983-128922320 | Common:1; Rare:76 | ||||
chr9:128947567-128947728 | Common:1; Rare:74; Clinvar:5; Clinvar (benign):1 | ||||
chr9:129110671-129110950 | Common:3; Rare:62 | ||||
chr9:129835218-129835478 | Common:2; Rare:105 | ||||
chr9:130053860-130053963 | Common:1; Rare:43 | ||||
chr9:131125446-131125637 | Common:1; Rare:89 | ||||
chr9:132354950-132355246 | Common:4; Rare:98 |