| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:17682241-17682508 | Common:1; Rare:80 | ||||
| chr17:17682518-17682586 | Rare:22 | ||||
| chr17:17682786-17682951 | Common:3; Rare:44 | ||||
| chr17:17682969-17683284 | Rare:88 | ||||
| chr17:17823594-17823897 | Common:5; Rare:121 | ||||
| chr17:17836335-17836687 | Common:2; Rare:78 | ||||
| chr17:17836722-17837057 | Common:3; Rare:85 | ||||
| chr17:17971972-17972094 | Common:2; Rare:29 | ||||
| chr17:17972571-17973053 | Common:5; Rare:121 | ||||
| chr17:17973082-17973125 | Rare:3 | ||||
| chr17:18039072-18039549 | Common:5; Rare:123; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:18039742-18040067 | Rare:78 | ||||
| chr17:18087663-18088019 | Rare:90 | ||||
| chr17:18088294-18088372 | Rare:17 | ||||
| chr17:18153844-18154054 | Common:4; Rare:52; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):2 |