| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:1762700-1762823 | Common:2; Rare:34 | ||||
| chr17:1771590-1771790 | Rare:50 | ||||
| chr17:1783901-1784224 | Common:1; Rare:70 | ||||
| chr17:1829791-1830071 | Common:8; Rare:118 | ||||
| chr17:2303450-2303637 | Rare:69 | ||||
| chr17:2303719-2304017 | Common:2; Rare:111 | ||||
| chr17:2336423-2336518 | Rare:35 | ||||
| chr17:2337353-2337631 | Common:1; Rare:83 | ||||
| chr17:2376000-2376182 | Common:1; Rare:61 | ||||
| chr17:2388009-2388323 | Common:1; Rare:77 | ||||
| chr17:2396786-2397031 | Common:2; Rare:53 | ||||
| chr17:2511766-2512021 | Common:2; Rare:74 | ||||
| chr17:2593441-2593697 | Common:4; Rare:102; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:2593852-2594191 | Common:1; Rare:99; Clinvar:4; Clinvar (benign):3 | ||||
| chr17:2711769-2712031 | Common:2; Rare:72 |