| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:47694426-47694609 | Common:6; Rare:51 | ||||
| chr17:47821744-47821906 | Common:1; Rare:36 | ||||
| chr17:47831479-47831631 | Rare:49 | ||||
| chr17:47841120-47841455 | Rare:73 | ||||
| chr17:47896477-47896565 | Rare:21 | ||||
| chr17:47941328-47941712 | Rare:103; Clinvar:5; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr17:47970740-47971171 | Common:4; Rare:102 | ||||
| chr17:48048039-48048400 | Common:1; Rare:98 | ||||
| chr17:48048602-48048813 | Common:4; Rare:30 | ||||
| chr17:48100816-48101529 | Common:4; Rare:183 | ||||
| chr17:48107427-48107817 | Common:5; Rare:94 | ||||
| chr17:48830931-48831059 | Common:2; Rare:38 | ||||
| chr17:48892298-48892522 | Common:10; Rare:75 | ||||
| chr17:48892570-48892857 | Common:3; Rare:78 | ||||
| chr17:48944715-48944918 | Common:2; Rare:72 |