| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:36544796-36544961 | Common:2; Rare:52 | ||||
| chr17:37406799-37406924 | Rare:50 | ||||
| chr17:37609351-37609561 | Common:1; Rare:88 | ||||
| chr17:37643416-37643488 | Rare:33 | ||||
| chr17:37744571-37744711 | Rare:58; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr17:37745057-37745183 | Rare:33; Clinvar (benign):2 | ||||
| chr17:38428300-38428482 | Common:8; Rare:69 | ||||
| chr17:38706096-38706149 | Rare:27 | ||||
| chr17:38749813-38749922 | Rare:19 | ||||
| chr17:38825285-38825408 | Common:2; Rare:36 | ||||
| chr17:38853696-38853787 | Common:2; Rare:41 | ||||
| chr17:38869866-38870203 | Common:4; Rare:106 | ||||
| chr17:38890382-38890447 | Rare:17 | ||||
| chr17:39401638-39401810 | Common:1; Rare:50 | ||||
| chr17:39451241-39451373 | Common:2; Rare:46 |