Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:27294273-27294352 | Common:1; Rare:22 | ||||
chr17:27294361-27294425 | Rare:17 | ||||
chr17:28335376-28335841 | Common:1; Rare:112 | ||||
chr17:28357355-28357691 | Common:10; Rare:158; Clinvar (pathogenic):1 | ||||
chr17:28371582-28371706 | Common:2; Rare:21 | ||||
chr17:28599007-28599162 | Common:2; Rare:41 | ||||
chr17:28645078-28645314 | Common:1; Rare:91 | ||||
chr17:28661848-28661941 | Rare:44 | ||||
chr17:28662115-28662327 | Rare:84 | ||||
chr17:28717782-28717943 | Rare:35 | ||||
chr17:28728726-28728807 | Rare:30 | ||||
chr17:28812370-28812667 | Common:1; Rare:78 | ||||
chr17:28854971-28855032 | Rare:16 | ||||
chr17:28897540-28897763 | Common:1; Rare:72 | ||||
chr17:29140368-29140470 | Common:3; Rare:35 |