| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:42423111-42423462 | Common:1; Rare:91; Clinvar:2 | ||||
| chr17:42458705-42458948 | Common:3; Rare:89 | ||||
| chr17:42577671-42577844 | Rare:85 | ||||
| chr17:42609333-42609732 | Common:8; Rare:165; Clinvar (benign):2 | ||||
| chr17:42745023-42745107 | Common:2; Rare:28 | ||||
| chr17:42760974-42761254 | Rare:72 | ||||
| chr17:42773369-42773475 | Rare:30 | ||||
| chr17:42798639-42798767 | Rare:41 | ||||
| chr17:42833340-42833472 | Rare:50 | ||||
| chr17:42964425-42964503 | Rare:34 | ||||
| chr17:42998372-42998522 | Common:4; Rare:47 | ||||
| chr17:43125359-43125621 | Rare:50; Clinvar:3; Clinvar (benign):2 | ||||
| chr17:43170292-43170479 | Common:2; Rare:37 | ||||
| chr17:43171008-43171233 | Rare:70 | ||||
| chr17:43398881-43398996 | Common:1; Rare:33 |