Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:174522429-174522613 | Rare:61; Clinvar:2; Clinvar (pathogenic):1 | ||||
chr4:177442354-177442519 | Rare:98; Clinvar:2; Clinvar (pathogenic):1 | ||||
chr4:183505972-183506110 | Rare:54 | ||||
chr4:183658994-183659395 | Common:1; Rare:118 | ||||
chr4:184474504-184474817 | Rare:70 | ||||
chr4:184649413-184649775 | Common:4; Rare:120 | ||||
chr4:184805518-184805854 | Common:2; Rare:61 | ||||
chr4:185143033-185143274 | Common:3; Rare:69; Clinvar (benign):2 | ||||
chr4:185203915-185204254 | Common:3; Rare:113 | ||||
chr4:185396574-185396843 | Rare:84 | ||||
chr4:185425875-185426006 | Common:2; Rare:51 | ||||
chr4:189940598-189940991 | Common:13; Rare:135 | ||||
chr5:218134-218360 | Common:3; Rare:89; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
chr5:443103-443269 | Common:9; Rare:73 | ||||
chr5:892647-892929 | Common:5; Rare:99 |