Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:28661812-28661964 | Common:1; Rare:63 | ||||
chr17:28662106-28662325 | Rare:89 | ||||
chr17:28717760-28717995 | Rare:50 | ||||
chr17:28718121-28718241 | Rare:31 | ||||
chr17:28727944-28728041 | Rare:25 | ||||
chr17:28728731-28728826 | Rare:36; Clinvar (benign):1 | ||||
chr17:28812378-28812641 | Common:1; Rare:67 | ||||
chr17:28842714-28842872 | Common:1; Rare:60 | ||||
chr17:28854976-28855032 | Rare:15 | ||||
chr17:28897590-28897737 | Common:1; Rare:53 | ||||
chr17:28949725-28949782 | Rare:13 | ||||
chr17:28951445-28951798 | Common:2; Rare:87 | ||||
chr17:29140363-29140484 | Common:3; Rare:39 | ||||
chr17:29294005-29294297 | Common:2; Rare:126 | ||||
chr17:29390107-29390461 | Common:3; Rare:101 |