Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:16215522-16215614 | Rare:35 | ||||
chr17:18039142-18039398 | Common:3; Rare:61; Clinvar (benign):1 | ||||
chr17:18314928-18315345 | Common:1; Rare:121 | ||||
chr17:18781117-18781301 | Common:3; Rare:50 | ||||
chr17:19377905-19378035 | Common:1; Rare:30 | ||||
chr17:19378156-19378599 | Common:2; Rare:102 | ||||
chr17:21214094-21214347 | Common:2; Rare:116 | ||||
chr17:28335376-28335690 | Common:1; Rare:74 | ||||
chr17:28357455-28357679 | Common:5; Rare:112 | ||||
chr17:28661812-28661947 | Common:1; Rare:58 | ||||
chr17:28662111-28662291 | Rare:77 | ||||
chr17:28717813-28718002 | Rare:38 | ||||
chr17:28725672-28725877 | Common:1; Rare:53 | ||||
chr17:29566973-29567295 | Rare:78 | ||||
chr17:29567974-29568135 | Rare:28 |