Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:1491608-1491816 | Common:1; Rare:63 | ||||
chr17:1516582-1516958 | Common:2; Rare:133 | ||||
chr17:1645698-1645858 | Common:2; Rare:44 | ||||
chr17:1676004-1676275 | Rare:53; Clinvar (benign):2 | ||||
chr17:1716192-1716490 | Common:1; Rare:90 | ||||
chr17:1829786-1830083 | Common:8; Rare:126 | ||||
chr17:2071457-2071813 | Common:4; Rare:90 | ||||
chr17:2303461-2303633 | Rare:63 | ||||
chr17:2303716-2303987 | Common:2; Rare:103 | ||||
chr17:2336430-2336533 | Rare:38 | ||||
chr17:2593464-2593680 | Common:3; Rare:81; Clinvar (benign):2 | ||||
chr17:3636235-3636517 | Common:4; Rare:82; Clinvar (benign):1 | ||||
chr17:3668522-3668845 | Common:3; Rare:133 | ||||
chr17:3723797-3723938 | Common:1; Rare:79 | ||||
chr17:4142985-4143249 | Rare:93 |