Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:16438672-16439058 | Common:1; Rare:95 | ||||
chr17:16981382-16981653 | Common:2; Rare:50 | ||||
chr17:16988333-16988496 | Rare:46 | ||||
chr17:17752193-17752405 | Common:1; Rare:76 | ||||
chr17:17836272-17836449 | Common:2; Rare:38 | ||||
chr17:21008387-21008648 | Common:3; Rare:67 | ||||
chr17:28737972-28738245 | Common:1; Rare:88; Clinvar:5; Clinvar (benign):1 | ||||
chr17:28891722-28891756 | Rare:2 | ||||
chr17:29099636-29099960 | Common:1; Rare:61 | ||||
chr17:29760509-29760565 | Rare:6 | ||||
chr17:30731405-30731705 | Common:3; Rare:89 | ||||
chr17:31319345-31319582 | Common:2; Rare:36 | ||||
chr17:32523450-32523572 | Rare:23 | ||||
chr17:35567891-35568151 | Common:2; Rare:77 | ||||
chr17:36518197-36518484 | Common:2; Rare:38 |