Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr8:106060441-106060540 | Rare:25 | ||||
chr8:124815749-124815812 | Common:1; Rare:21 | ||||
chr8:127737528-127737774 | Common:2; Rare:64 | ||||
chr8:127794372-127794575 | Rare:54 | ||||
chr8:145002827-145003010 | Common:2; Rare:60 | ||||
chr9:693502-693689 | Rare:49 | ||||
chr9:21559828-21559925 | Rare:58 | ||||
chr9:35341753-35341844 | Rare:18 | ||||
chr9:35657724-35657764 | Common:1; Rare:26; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr9:39464494-39464657 | Rare:37 | ||||
chr9:40992021-40992385 | Common:7; Rare:27 | ||||
chr9:62802073-62802177 | |||||
chr9:63859635-63859717 | Common:1; Rare:3 | ||||
chr9:66269890-66270047 | Common:1; Rare:29 | ||||
chr9:70413420-70413617 | Rare:64 |