| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:1400070-1400356 | Common:3; Rare:121 | ||||
| chr17:1491612-1491852 | Common:1; Rare:72 | ||||
| chr17:1516588-1516960 | Common:2; Rare:130 | ||||
| chr17:1716245-1716550 | Common:3; Rare:92 | ||||
| chr17:1762663-1762826 | Common:3; Rare:36 | ||||
| chr17:1829786-1830038 | Common:6; Rare:108 | ||||
| chr17:2303450-2303588 | Rare:50 | ||||
| chr17:2303728-2303987 | Common:2; Rare:97 | ||||
| chr17:2336430-2336518 | Rare:31 | ||||
| chr17:2593441-2593664 | Common:3; Rare:90 | ||||
| chr17:2593863-2593970 | Common:1; Rare:32; Clinvar:1; Clinvar (benign):3 | ||||
| chr17:2711767-2712028 | Common:2; Rare:72 | ||||
| chr17:3471765-3471890 | Common:6; Rare:45 | ||||
| chr17:3636231-3636486 | Common:4; Rare:75; Clinvar (benign):1 | ||||
| chr17:3636698-3636779 | Common:1; Rare:22; Clinvar (benign):1 |