| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:2303713-2304001 | Common:2; Rare:110 | ||||
| chr17:2336335-2336515 | Rare:81 | ||||
| chr17:2337395-2337519 | Rare:34 | ||||
| chr17:2511754-2511924 | Common:2; Rare:41 | ||||
| chr17:2593467-2593701 | Common:3; Rare:89; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:3636234-3636489 | Common:4; Rare:75; Clinvar (benign):1 | ||||
| chr17:3668522-3668822 | Common:3; Rare:121 | ||||
| chr17:3723772-3723900 | Common:1; Rare:72 | ||||
| chr17:4143001-4143232 | Rare:75 | ||||
| chr17:4143605-4143740 | Common:4; Rare:77 | ||||
| chr17:4263943-4264212 | Common:2; Rare:85 | ||||
| chr17:4555326-4555510 | Common:3; Rare:84 | ||||
| chr17:4704111-4704250 | Rare:77 | ||||
| chr17:4807070-4807203 | Common:2; Rare:41 | ||||
| chr17:4939909-4940338 | Common:2; Rare:127 |