| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:3916406-3916662 | Common:1; Rare:51 | ||||
| chr17:4142967-4143235 | Common:3; Rare:92 | ||||
| chr17:4143605-4143744 | Common:4; Rare:81 | ||||
| chr17:4263943-4264042 | Rare:43 | ||||
| chr17:4555334-4555503 | Common:3; Rare:75 | ||||
| chr17:4704114-4704269 | Rare:79 | ||||
| chr17:4731268-4731481 | Common:2; Rare:62 | ||||
| chr17:4736338-4736557 | Rare:41 | ||||
| chr17:4738953-4739116 | Common:1; Rare:25 | ||||
| chr17:4739371-4739448 | Common:2; Rare:27 | ||||
| chr17:4739488-4739955 | Common:6; Rare:108 | ||||
| chr17:4797565-4797688 | Common:1; Rare:35 | ||||
| chr17:4807007-4807195 | Common:4; Rare:62 | ||||
| chr17:4899353-4899694 | Common:3; Rare:167; Clinvar:9; Clinvar (benign):7; Clinvar (pathogenic):3 | ||||
| chr17:4939912-4940394 | Common:2; Rare:143 |