| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:37744887-37745200 | Common:2; Rare:136; Clinvar:2; Clinvar (benign):6 | ||||
| chr17:37745230-37745420 | Rare:73 | ||||
| chr17:37745440-37745890 | Common:7; Rare:198 | ||||
| chr17:38296880-38297224 | Common:10; Rare:220 | ||||
| chr17:38351590-38352065 | Common:8; Rare:309 | ||||
| chr17:38559400-38559660 | Common:1; Rare:71 | ||||
| chr17:38604670-38605151 | Common:6; Rare:197 | ||||
| chr17:38605758-38606169 | Common:2; Rare:217 | ||||
| chr17:38606400-38606670 | Common:3; Rare:55 | ||||
| chr17:38674868-38675094 | Common:6; Rare:99 | ||||
| chr17:38705018-38705520 | Common:5; Rare:238 | ||||
| chr17:38706041-38706221 | Common:1; Rare:91 | ||||
| chr17:38730054-38730494 | Common:1; Rare:197 | ||||
| chr17:38746440-38746790 | Common:2; Rare:65 | ||||
| chr17:38747465-38747689 | Rare:41 |