Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr9:99221906-99222329 | Common:2; Rare:160; Clinvar:2; Clinvar (benign):2 | ||||
chr9:100098917-100099275 | Common:2; Rare:97 | ||||
chr9:100352913-100353071 | Rare:45 | ||||
chr9:101398594-101398863 | Rare:89 | ||||
chr9:108933947-108934477 | Common:8; Rare:209; Clinvar:7; Clinvar (benign):2 | ||||
chr9:109013452-109013852 | Common:3; Rare:132 | ||||
chr9:110256443-110256718 | Common:4; Rare:100 | ||||
chr9:111631143-111631386 | Common:1; Rare:68 | ||||
chr9:111661487-111661666 | Common:3; Rare:51 | ||||
chr9:112379780-112380138 | Common:4; Rare:139 | ||||
chr9:113221227-113221602 | Common:1; Rare:121 | ||||
chr9:113275578-113275697 | Common:2; Rare:45; Clinvar (pathogenic):1 | ||||
chr9:116153565-116153925 | Common:2; Rare:87 | ||||
chr9:116687228-116687376 | Common:1; Rare:46; Clinvar:2; Clinvar (benign):2 | ||||
chr9:120842978-120843104 | Rare:37 |