Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:1492631-1492795 | Rare:33 | ||||
chr17:1516566-1516960 | Common:2; Rare:143 | ||||
chr17:1673085-1673389 | Common:2; Rare:72; Clinvar:2 | ||||
chr17:1684780-1685031 | Common:2; Rare:85; Clinvar:7; Clinvar (benign):1 | ||||
chr17:1716129-1716492 | Common:1; Rare:111 | ||||
chr17:1762642-1762823 | Common:3; Rare:40 | ||||
chr17:1829786-1830043 | Common:8; Rare:110 | ||||
chr17:2214291-2214426 | Common:1; Rare:23 | ||||
chr17:2303305-2303375 | Rare:22 | ||||
chr17:2303450-2303594 | Rare:53 | ||||
chr17:2303709-2303981 | Common:2; Rare:106 | ||||
chr17:2336423-2336543 | Rare:47 | ||||
chr17:2396767-2397073 | Common:2; Rare:72 | ||||
chr17:2593470-2593677 | Common:3; Rare:76; Clinvar (benign):2 | ||||
chr17:2593818-2593990 | Common:1; Rare:45; Clinvar:3; Clinvar (benign):3 |