Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:1716179-1716536 | Common:3; Rare:112 | ||||
chr17:1829780-1830108 | Common:9; Rare:136 | ||||
chr17:2303709-2303988 | Common:2; Rare:106 | ||||
chr17:2336413-2336553 | Rare:58 | ||||
chr17:2593464-2593680 | Common:3; Rare:81; Clinvar (benign):2 | ||||
chr17:2593863-2593987 | Common:1; Rare:34; Clinvar:1; Clinvar (benign):3 | ||||
chr17:2711769-2712031 | Common:2; Rare:72 | ||||
chr17:3636235-3636560 | Common:5; Rare:92; Clinvar (benign):2 | ||||
chr17:3668552-3668861 | Common:2; Rare:126 | ||||
chr17:3723767-3723903 | Common:1; Rare:77 | ||||
chr17:3892955-3893248 | Common:3; Rare:101 | ||||
chr17:4142989-4143250 | Rare:92 | ||||
chr17:4143597-4143740 | Common:4; Rare:80 | ||||
chr17:4263943-4264096 | Rare:61 | ||||
chr17:4366360-4366447 | Rare:26 |