Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:28552550-28552756 | Rare:78; Clinvar:3; Clinvar (benign):1 | ||||
chr17:28571497-28571679 | Rare:41 | ||||
chr17:28598980-28599170 | Common:2; Rare:61 | ||||
chr17:28616503-28616761 | Common:1; Rare:66 | ||||
chr17:28645028-28645310 | Common:1; Rare:118 | ||||
chr17:28661848-28661948 | Rare:46 | ||||
chr17:28662157-28662325 | Rare:68 | ||||
chr17:28727822-28728041 | Common:1; Rare:46 | ||||
chr17:28728655-28728806 | Rare:57 | ||||
chr17:28743883-28744186 | Common:4; Rare:99 | ||||
chr17:28854958-28855173 | Rare:71 | ||||
chr17:28897050-28897222 | Rare:43 | ||||
chr17:28897540-28897734 | Common:1; Rare:65 | ||||
chr17:29042631-29042822 | Common:2; Rare:47 | ||||
chr17:29140379-29140484 | Common:3; Rare:35 |