Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:75205370-75205730 | Common:1; Rare:108 | ||||
chr17:75261583-75261945 | Common:4; Rare:115; Clinvar (benign):2 | ||||
chr17:75271146-75271369 | Common:2; Rare:42 | ||||
chr17:75289365-75289613 | Common:2; Rare:82; Clinvar:1; Clinvar (benign):2 | ||||
chr17:75393685-75394031 | Common:1; Rare:88 | ||||
chr17:75515427-75515647 | Common:3; Rare:65 | ||||
chr17:75667152-75667391 | Common:4; Rare:82 | ||||
chr17:75721179-75721550 | Common:3; Rare:114; Clinvar:1 | ||||
chr17:75784564-75784868 | Common:2; Rare:133 | ||||
chr17:75978990-75979283 | Rare:86; Clinvar:4; Clinvar (benign):1 | ||||
chr17:75979358-75979455 | Common:1; Rare:30; Clinvar (benign):1 | ||||
chr17:76072497-76072636 | Rare:41 | ||||
chr17:76501372-76501550 | Rare:65; Clinvar (benign):3 | ||||
chr17:76688627-76688914 | Common:5; Rare:59 | ||||
chr17:76725969-76726086 | Common:1; Rare:30 |