Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:75148541-75148769 | Rare:45 | ||||
chr17:75555946-75556141 | Common:5; Rare:69 | ||||
chr17:75685047-75685319 | Common:2; Rare:44 | ||||
chr17:75720688-75720776 | Rare:18 | ||||
chr17:75722113-75722311 | Rare:25 | ||||
chr17:75736045-75736383 | Common:2; Rare:93; Clinvar:5; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
chr17:75740036-75740401 | Common:3; Rare:104; Clinvar:1 | ||||
chr17:76015613-76015912 | Common:2; Rare:57 | ||||
chr17:76021916-76022212 | Common:1; Rare:91 | ||||
chr17:76023400-76023524 | Common:2; Rare:37 | ||||
chr17:76023626-76023886 | Rare:54 | ||||
chr17:76494952-76495146 | Common:1; Rare:35 | ||||
chr17:76557676-76557821 | Rare:51 | ||||
chr17:76563279-76563379 | Common:2; Rare:17 | ||||
chr17:78315542-78315720 | Rare:29 |