| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:1480570-1480879 | Common:2; Rare:101; Clinvar (benign):2 | ||||
| chr17:1516675-1516978 | Common:1; Rare:111 | ||||
| chr17:1628374-1628519 | Rare:39 | ||||
| chr17:1684794-1685048 | Common:2; Rare:80; Clinvar:4; Clinvar (benign):1 | ||||
| chr17:1716200-1716490 | Common:1; Rare:87 | ||||
| chr17:1829805-1830051 | Common:7; Rare:105 | ||||
| chr17:2303728-2303987 | Common:2; Rare:97 | ||||
| chr17:2336413-2336563 | Rare:61 | ||||
| chr17:2511778-2511975 | Common:2; Rare:54 | ||||
| chr17:2593850-2593987 | Common:1; Rare:39; Clinvar:3; Clinvar (benign):3 | ||||
| chr17:2711771-2712043 | Common:2; Rare:75 | ||||
| chr17:3636245-3636496 | Common:4; Rare:69; Clinvar (benign):1 | ||||
| chr17:3636662-3636772 | Common:1; Rare:28; Clinvar:2; Clinvar (benign):1 | ||||
| chr17:3668538-3668820 | Common:3; Rare:112 | ||||
| chr17:3723764-3723925 | Common:1; Rare:89 |