Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:21214148-21214349 | Common:2; Rare:92 | ||||
chr17:21574433-21574823 | Common:2; Rare:84 | ||||
chr17:27293953-27294140 | Common:1; Rare:82 | ||||
chr17:28335376-28335850 | Common:1; Rare:113 | ||||
chr17:28357438-28357722 | Common:5; Rare:139; Clinvar (pathogenic):1 | ||||
chr17:28571492-28571698 | Rare:51 | ||||
chr17:28645099-28645310 | Common:1; Rare:79 | ||||
chr17:28661881-28661941 | Rare:28 | ||||
chr17:28662166-28662316 | Rare:60 | ||||
chr17:28717601-28717995 | Common:2; Rare:90 | ||||
chr17:28719687-28720063 | Common:1; Rare:117 | ||||
chr17:28727944-28728041 | Rare:25 | ||||
chr17:28728718-28728811 | Rare:37 | ||||
chr17:28812405-28812577 | Common:1; Rare:46 | ||||
chr17:28842755-28842885 | Common:1; Rare:45 |