| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:1727175-1727480 | Common:1; Rare:76; Clinvar (benign):2 | ||||
| chr17:1829780-1830124 | Common:9; Rare:143 | ||||
| chr17:1843775-1843950 | Common:2; Rare:42 | ||||
| chr17:1879353-1879697 | Common:3; Rare:104 | ||||
| chr17:2041045-2041274 | Rare:80 | ||||
| chr17:2041444-2041514 | Common:1; Rare:30 | ||||
| chr17:2071586-2071675 | Rare:23 | ||||
| chr17:2214329-2214490 | Common:1; Rare:36 | ||||
| chr17:2240075-2240320 | Common:1; Rare:53 | ||||
| chr17:2244769-2244911 | Common:1; Rare:23 | ||||
| chr17:2303310-2303375 | Rare:20 | ||||
| chr17:2303423-2303640 | Rare:77 | ||||
| chr17:2303722-2304010 | Common:2; Rare:108 | ||||
| chr17:2336329-2336550 | Rare:100 | ||||
| chr17:2511753-2511975 | Common:2; Rare:57 |