Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr9:94332376-94332541 | Common:1; Rare:67 | ||||
chr9:94347452-94347535 | Rare:14 | ||||
chr9:94375334-94375418 | Common:1; Rare:21 | ||||
chr9:97012624-97012875 | Common:3; Rare:53 | ||||
chr9:97674750-97674983 | Common:1; Rare:59 | ||||
chr9:97687232-97687414 | Common:1; Rare:39; Clinvar:1; Clinvar (pathogenic):1 | ||||
chr9:99819490-99819611 | Rare:39 | ||||
chr9:99819967-99820321 | Common:1; Rare:91 | ||||
chr9:104778991-104779156 | Rare:27 | ||||
chr9:104841758-104842082 | Common:3; Rare:53 | ||||
chr9:104858923-104859117 | Rare:35 | ||||
chr9:104903677-104903972 | Common:3; Rare:67; Clinvar (benign):4 | ||||
chr9:104905999-104906126 | Rare:23 | ||||
chr9:104907248-104907530 | Common:2; Rare:58 | ||||
chr9:104926566-104926805 | Common:6; Rare:66 |