| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:1109737-1109761 | Rare:4 | ||||
| chr17:1345448-1345774 | Common:1; Rare:92 | ||||
| chr17:1355065-1355109 | Rare:5 | ||||
| chr17:1363764-1363803 | Rare:7 | ||||
| chr17:1370182-1370266 | Common:3; Rare:30 | ||||
| chr17:1394036-1394179 | Common:1; Rare:44 | ||||
| chr17:1437113-1437221 | Rare:34 | ||||
| chr17:1487923-1488217 | Common:4; Rare:82 | ||||
| chr17:1523881-1524028 | Common:1; Rare:32 | ||||
| chr17:1535185-1535483 | Rare:94 | ||||
| chr17:1625874-1625953 | Rare:10 | ||||
| chr17:1658250-1658611 | Rare:74; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:1711546-1711758 | Rare:34 | ||||
| chr17:1711761-1712210 | Common:1; Rare:89 | ||||
| chr17:1712337-1712392 | Rare:20 |