Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:2593856-2594001 | Common:1; Rare:38; Clinvar:3; Clinvar (benign):3 | ||||
chr17:2711787-2712031 | Common:2; Rare:63 | ||||
chr17:3636226-3636501 | Common:4; Rare:84; Clinvar (benign):1 | ||||
chr17:3668552-3668820 | Common:2; Rare:104 | ||||
chr17:3723797-3723887 | Common:1; Rare:48 | ||||
chr17:4142998-4143244 | Rare:81 | ||||
chr17:4143597-4143735 | Common:4; Rare:79 | ||||
chr17:4263934-4264072 | Rare:56 | ||||
chr17:4555312-4555503 | Common:3; Rare:88 | ||||
chr17:4560537-4560651 | Rare:28 | ||||
chr17:4704079-4704250 | Rare:92 | ||||
chr17:4710615-4710709 | Rare:32 | ||||
chr17:4739542-4739573 | Rare:8 | ||||
chr17:4739870-4740010 | Rare:33 | ||||
chr17:4806982-4807210 | Common:4; Rare:72 |