Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:18039091-18039410 | Common:3; Rare:80; Clinvar:1; Clinvar (benign):1 | ||||
chr17:18314923-18315380 | Common:1; Rare:134 | ||||
chr17:18315693-18315990 | Rare:96 | ||||
chr17:18780982-18781283 | Common:6; Rare:77 | ||||
chr17:18857926-18858186 | Common:5; Rare:64 | ||||
chr17:19377640-19377775 | Common:2; Rare:36 | ||||
chr17:19377905-19378044 | Common:1; Rare:31 | ||||
chr17:19378148-19378585 | Common:2; Rare:101 | ||||
chr17:19648005-19648200 | Rare:43 | ||||
chr17:19977828-19978143 | Common:2; Rare:87 | ||||
chr17:21214123-21214368 | Common:2; Rare:113 | ||||
chr17:21287843-21288054 | Rare:58 | ||||
chr17:27293919-27294149 | Common:2; Rare:100 | ||||
chr17:27643529-27643961 | Common:9; Rare:101 | ||||
chr17:28329226-28329342 | Rare:40 |