Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr9:19229634-19229885 | Common:1; Rare:63 | ||||
chr9:19378366-19378920 | Common:1; Rare:163 | ||||
chr9:32550821-32551187 | Common:1; Rare:145; Clinvar:2; Clinvar (benign):2 | ||||
chr9:33677086-33677250 | Common:5; Rare:47 | ||||
chr9:34158590-34158822 | Common:1; Rare:45 | ||||
chr9:35604027-35604177 | Common:3; Rare:37 | ||||
chr9:35604225-35604427 | Rare:49 | ||||
chr9:35657724-35657764 | Common:1; Rare:26; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr9:35728269-35728450 | Rare:33 | ||||
chr9:37079796-37080027 | Common:4; Rare:75 | ||||
chr9:39809339-39809531 | Common:4; Rare:15 | ||||
chr9:39809672-39809759 | Common:2; Rare:8 | ||||
chr9:39809792-39809836 | Rare:2 | ||||
chr9:40992072-40992420 | Common:7; Rare:24 | ||||
chr9:41274004-41274274 | Common:2; Rare:33 |