Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:15427477-15427623 | Common:1; Rare:51 | ||||
chr3:15601401-15601801 | Common:4; Rare:166; Clinvar:1 | ||||
chr3:15796816-15796963 | Common:1; Rare:21 | ||||
chr3:15797009-15797388 | Common:6; Rare:77 | ||||
chr3:15859735-15860114 | Common:4; Rare:124 | ||||
chr3:16264851-16265268 | Common:3; Rare:144 | ||||
chr3:19946978-19947415 | Common:5; Rare:165 | ||||
chr3:20186138-20186370 | Common:3; Rare:67 | ||||
chr3:23916893-23917214 | Rare:123 | ||||
chr3:25783380-25783628 | Common:2; Rare:82; Clinvar (benign):3 | ||||
chr3:28348986-28349168 | Common:2; Rare:55 | ||||
chr3:29280806-29281092 | Common:3; Rare:58 | ||||
chr3:31532394-31532703 | Common:4; Rare:91 | ||||
chr3:31981600-31981766 | Rare:44 | ||||
chr3:32570775-32570952 | Common:1; Rare:86 |