| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:1179966-1180117 | Common:9; Rare:27 | ||||
| chr17:1400049-1400304 | Common:2; Rare:98 | ||||
| chr17:1400353-1400491 | Common:1; Rare:41 | ||||
| chr17:1456180-1456458 | Common:4; Rare:101 | ||||
| chr17:1478220-1478347 | Common:2; Rare:25 | ||||
| chr17:1478380-1478734 | Common:2; Rare:136; Clinvar (benign):2 | ||||
| chr17:1480609-1480789 | Common:1; Rare:56 | ||||
| chr17:1485707-1486073 | Common:5; Rare:122 | ||||
| chr17:1491608-1491769 | Common:1; Rare:47 | ||||
| chr17:1516566-1516954 | Common:2; Rare:140 | ||||
| chr17:1562521-1562638 | Common:1; Rare:27 | ||||
| chr17:1628395-1628471 | Rare:15 | ||||
| chr17:1675965-1676301 | Common:1; Rare:63; Clinvar (benign):4 | ||||
| chr17:1684773-1685036 | Common:2; Rare:91; Clinvar:7; Clinvar (benign):1 | ||||
| chr17:1716134-1716588 | Common:4; Rare:146 |