Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:19648609-19649010 | Common:3; Rare:139; Clinvar (benign):1 | ||||
chr17:19977804-19977936 | Common:1; Rare:42 | ||||
chr17:21043399-21043514 | Common:1; Rare:43 | ||||
chr17:21214123-21214361 | Common:2; Rare:110 | ||||
chr17:27293958-27294173 | Common:2; Rare:90 | ||||
chr17:27294283-27294479 | Common:2; Rare:55 | ||||
chr17:28335347-28335836 | Common:1; Rare:117 | ||||
chr17:28357410-28357679 | Common:6; Rare:133 | ||||
chr17:28571462-28571642 | Rare:57 | ||||
chr17:28598970-28599174 | Common:2; Rare:65 | ||||
chr17:28645099-28645310 | Common:1; Rare:79 | ||||
chr17:28661881-28661941 | Rare:28 | ||||
chr17:28662132-28662337 | Rare:81 | ||||
chr17:28719655-28720030 | Common:1; Rare:103 | ||||
chr17:28728670-28728811 | Rare:57 |