| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:1493104-1493334 | Rare:47 | ||||
| chr17:1516582-1517008 | Common:2; Rare:147 | ||||
| chr17:1628374-1628469 | Rare:19 | ||||
| chr17:1628793-1628847 | Rare:18 | ||||
| chr17:1645720-1645907 | Common:2; Rare:41 | ||||
| chr17:1684780-1685064 | Common:2; Rare:95; Clinvar:7; Clinvar (benign):1 | ||||
| chr17:1716128-1716544 | Common:3; Rare:129 | ||||
| chr17:1762580-1762843 | Common:4; Rare:55 | ||||
| chr17:1776948-1777291 | Common:1; Rare:117; Clinvar:1 | ||||
| chr17:1783755-1784203 | Common:2; Rare:91 | ||||
| chr17:1829779-1830051 | Common:8; Rare:115 | ||||
| chr17:2041411-2041541 | Common:1; Rare:52 | ||||
| chr17:2214282-2214572 | Common:1; Rare:56 | ||||
| chr17:2303434-2303592 | Rare:56 | ||||
| chr17:2303713-2303980 | Common:2; Rare:103 |