Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:176319721-176320042 | Common:4; Rare:111 | ||||
chr4:177442376-177442514 | Rare:83; Clinvar:2 | ||||
chr4:182144453-182144719 | Common:3; Rare:83 | ||||
chr4:183444327-183444664 | Common:2; Rare:138 | ||||
chr4:183505931-183506116 | Common:1; Rare:70 | ||||
chr4:183658985-183659401 | Common:1; Rare:127 | ||||
chr4:184474504-184474817 | Rare:70 | ||||
chr4:184649386-184649796 | Common:5; Rare:133 | ||||
chr4:184734048-184734383 | Common:5; Rare:126 | ||||
chr4:185203915-185204172 | Common:2; Rare:87 | ||||
chr4:185396581-185396855 | Rare:87 | ||||
chr4:185425878-185426283 | Common:4; Rare:120 | ||||
chr4:185535453-185535630 | Common:1; Rare:59; Clinvar (benign):2 | ||||
chr4:186723759-186724034 | Common:9; Rare:103 | ||||
chr4:189940631-189941012 | Common:14; Rare:142 |