Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:737578-737851 | Common:1; Rare:53 | ||||
chr17:909606-909897 | Common:4; Rare:69 | ||||
chr17:1714096-1714410 | Common:2; Rare:55 | ||||
chr17:1747141-1747281 | Rare:46 | ||||
chr17:3664932-3665186 | Common:2; Rare:32 | ||||
chr17:4529165-4529406 | Rare:49 | ||||
chr17:4546973-4547125 | Rare:30 | ||||
chr17:4858943-4859276 | Common:1; Rare:67 | ||||
chr17:4873680-4873688 | |||||
chr17:4886137-4886615 | Common:1; Rare:98 | ||||
chr17:4945494-4945869 | Common:2; Rare:130 | ||||
chr17:5003670-5003927 | Common:1; Rare:73; Clinvar (benign):1 | ||||
chr17:5434907-5435209 | Common:2; Rare:63 | ||||
chr17:6998484-6998755 | Rare:72 | ||||
chr17:7046909-7047077 | Common:1; Rare:38 |