Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr9:19378395-19378798 | Common:1; Rare:120 | ||||
chr9:20732222-20732453 | Common:1; Rare:45 | ||||
chr9:25677399-25677708 | Common:4; Rare:133 | ||||
chr9:32550845-32551156 | Common:1; Rare:124; Clinvar:2; Clinvar (benign):2 | ||||
chr9:33816257-33816517 | Common:1; Rare:45 | ||||
chr9:37087329-37087549 | Rare:43 | ||||
chr9:40992075-40992362 | Common:7; Rare:24 | ||||
chr9:41358807-41358926 | Common:1; Rare:35 | ||||
chr9:62802625-62802781 | |||||
chr9:66270428-66270494 | Common:12; Rare:20 | ||||
chr9:69008170-69008584 | Rare:98 | ||||
chr9:70420087-70420288 | Common:3; Rare:52 | ||||
chr9:73158597-73158740 | Rare:48 | ||||
chr9:78031995-78032116 | Rare:47 | ||||
chr9:83979579-83979604 | Rare:10 |