| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:39637024-39637159 | Common:2; Rare:40 | ||||
| chr17:39688022-39688125 | Rare:33 | ||||
| chr17:39927513-39927732 | Common:2; Rare:66 | ||||
| chr17:40140153-40140548 | Common:5; Rare:185 | ||||
| chr17:41812655-41813029 | Common:2; Rare:86; Clinvar:5 | ||||
| chr17:41966606-41966831 | Common:1; Rare:81 | ||||
| chr17:42017382-42017483 | Rare:46 | ||||
| chr17:42423093-42423413 | Common:1; Rare:85; Clinvar:2 | ||||
| chr17:42458738-42458926 | Common:2; Rare:73 | ||||
| chr17:42577664-42577825 | Rare:74 | ||||
| chr17:42609330-42609732 | Common:8; Rare:167; Clinvar (benign):2 | ||||
| chr17:42773371-42773484 | Rare:35 | ||||
| chr17:42833093-42833497 | Rare:117 | ||||
| chr17:42964422-42964534 | Rare:53 | ||||
| chr17:43125345-43125654 | Rare:74; Clinvar:3; Clinvar (benign):2 |