Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:48583771-48583987 | Rare:70 | ||||
chr3:48592857-48593157 | Rare:94; Clinvar:4; Clinvar (pathogenic):3 | ||||
chr3:49132117-49132375 | Common:1; Rare:71; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr3:50008850-50009077 | Common:2; Rare:36 | ||||
chr3:50627439-50627842 | Common:1; Rare:76 | ||||
chr3:50654973-50654989 | Rare:2 | ||||
chr3:50664469-50664693 | Rare:30 | ||||
chr3:51392158-51392393 | Rare:88 | ||||
chr3:51393904-51393984 | Rare:20 | ||||
chr3:52482263-52482412 | Common:1; Rare:40 | ||||
chr3:57557015-57557106 | Rare:28 | ||||
chr3:64005657-64005761 | Rare:17 | ||||
chr3:64014657-64014816 | Common:1; Rare:36 | ||||
chr3:66385895-66385908 | Rare:5 | ||||
chr3:75435048-75435395 | Common:4; Rare:122 |