Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:18781103-18781332 | Common:5; Rare:65 | ||||
chr17:18856168-18856362 | Common:1; Rare:35 | ||||
chr17:19004132-19004290 | Rare:35 | ||||
chr17:19004729-19004878 | Common:1; Rare:51 | ||||
chr17:19378189-19378499 | Common:1; Rare:73 | ||||
chr17:19648609-19649122 | Common:3; Rare:185; Clinvar (benign):1 | ||||
chr17:19977789-19977945 | Common:1; Rare:53 | ||||
chr17:21214144-21214341 | Common:2; Rare:87 | ||||
chr17:27294008-27294132 | Common:1; Rare:49 | ||||
chr17:28335371-28335850 | Common:1; Rare:113 | ||||
chr17:28357351-28357679 | Common:10; Rare:151 | ||||
chr17:28368166-28368414 | Rare:42 | ||||
chr17:28368519-28369030 | Common:3; Rare:165 | ||||
chr17:28369916-28370435 | Common:1; Rare:129 | ||||
chr17:28370458-28370746 | Common:2; Rare:63 |