Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:2593863-2593970 | Common:1; Rare:32; Clinvar:1; Clinvar (benign):3 | ||||
chr17:2711787-2712028 | Common:2; Rare:63 | ||||
chr17:3668552-3668837 | Common:2; Rare:112 | ||||
chr17:3695420-3695655 | Rare:38 | ||||
chr17:3723772-3723922 | Common:1; Rare:82 | ||||
chr17:4143020-4143244 | Rare:69 | ||||
chr17:4143603-4143727 | Common:4; Rare:72 | ||||
chr17:4263943-4264042 | Rare:43 | ||||
chr17:4555329-4555503 | Common:3; Rare:80 | ||||
chr17:4704116-4704250 | Rare:74 | ||||
chr17:4731316-4731482 | Common:2; Rare:50 | ||||
chr17:4807008-4807192 | Common:4; Rare:62 | ||||
chr17:4939916-4940136 | Common:2; Rare:74 | ||||
chr17:4950433-4950591 | Rare:35 | ||||
chr17:4951540-4951776 | Rare:49 |