Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr9:122828484-122828768 | Rare:83 | ||||
chr9:125143463-125143687 | Rare:93 | ||||
chr9:125189753-125190050 | Common:1; Rare:114 | ||||
chr9:125240780-125241097 | Rare:86 | ||||
chr9:125241233-125241673 | Common:2; Rare:126 | ||||
chr9:127122321-127122342 | Rare:3 | ||||
chr9:127451371-127451571 | Common:2; Rare:65; Clinvar (benign):1 | ||||
chr9:127612002-127612394 | Common:2; Rare:142; Clinvar:4; Clinvar (benign):3 | ||||
chr9:127877667-127877775 | Rare:22 | ||||
chr9:127950737-127951043 | Common:2; Rare:64 | ||||
chr9:128191435-128191744 | Common:1; Rare:85 | ||||
chr9:128275909-128276293 | Common:4; Rare:167 | ||||
chr9:128552395-128552693 | Rare:113; Clinvar:6; Clinvar (benign):3 | ||||
chr9:128656635-128657034 | Common:2; Rare:127; Clinvar (pathogenic):1 | ||||
chr9:128683533-128683913 | Rare:85 |