Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr9:19102893-19103090 | Common:2; Rare:83 | ||||
chr9:20684086-20684282 | Common:3; Rare:77 | ||||
chr9:26892738-26892866 | Rare:66 | ||||
chr9:26947146-26947207 | Rare:21 | ||||
chr9:33001568-33001721 | Common:2; Rare:82; Clinvar (benign):3 | ||||
chr9:33025090-33025339 | Common:7; Rare:107 | ||||
chr9:33290394-33290563 | Common:2; Rare:63 | ||||
chr9:34048880-34048992 | Common:1; Rare:45 | ||||
chr9:34126651-34126781 | Rare:40 | ||||
chr9:34329250-34329620 | Common:1; Rare:109 | ||||
chr9:34665384-34665672 | Rare:90 | ||||
chr9:35103100-35103157 | Common:1; Rare:25 | ||||
chr9:35103160-35103297 | Rare:37 | ||||
chr9:35657970-35658322 | Common:5; Rare:277; Clinvar:20; Clinvar (benign):11; Clinvar (pathogenic):34 | ||||
chr9:35732083-35732320 | Common:1; Rare:66 |