| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:1279455-1279827 | Common:2; Rare:93 | ||||
| chr17:1279856-1279920 | Common:1; Rare:18 | ||||
| chr17:1400037-1400345 | Common:3; Rare:126 | ||||
| chr17:1480576-1480878 | Common:2; Rare:98; Clinvar (benign):1 | ||||
| chr17:1491608-1491811 | Common:1; Rare:63 | ||||
| chr17:1492563-1492707 | Common:1; Rare:25 | ||||
| chr17:1516582-1517008 | Common:2; Rare:147 | ||||
| chr17:1628809-1628847 | Rare:11 | ||||
| chr17:1645710-1645858 | Common:2; Rare:40 | ||||
| chr17:1716179-1716543 | Common:3; Rare:113 | ||||
| chr17:1762811-1762823 | Rare:1 | ||||
| chr17:1776375-1776741 | Common:7; Rare:111; Clinvar:2; Clinvar (benign):1 | ||||
| chr17:1783763-1784034 | Common:1; Rare:48 | ||||
| chr17:1829792-1830038 | Common:6; Rare:106 | ||||
| chr17:2029925-2030166 | Common:3; Rare:83 |