| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:4263943-4264037 | Rare:41 | ||||
| chr17:4541509-4541829 | Common:4; Rare:127 | ||||
| chr17:4542480-4542658 | Rare:85 | ||||
| chr17:4555320-4555533 | Common:3; Rare:99 | ||||
| chr17:4704093-4704231 | Rare:73 | ||||
| chr17:4731283-4731484 | Common:2; Rare:60 | ||||
| chr17:4738786-4739099 | Common:2; Rare:73 | ||||
| chr17:4739330-4739622 | Common:6; Rare:85 | ||||
| chr17:4771754-4772027 | Common:2; Rare:77 | ||||
| chr17:4786358-4786422 | Rare:18 | ||||
| chr17:4796027-4796276 | Common:2; Rare:90 | ||||
| chr17:4806994-4807192 | Common:4; Rare:65 | ||||
| chr17:4899360-4899575 | Common:2; Rare:121; Clinvar:9; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr17:4939827-4940396 | Common:2; Rare:166 | ||||
| chr17:4940907-4941110 | Rare:69 |