| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:35809194-35809599 | Common:1; Rare:155 | ||||
| chr17:36001451-36001675 | Common:1; Rare:47 | ||||
| chr17:36090133-36090402 | Common:1; Rare:54 | ||||
| chr17:36103825-36103833 | Rare:1 | ||||
| chr17:36486476-36486702 | Common:2; Rare:74 | ||||
| chr17:36534780-36535034 | Common:3; Rare:108 | ||||
| chr17:36544761-36544997 | Common:4; Rare:79 | ||||
| chr17:36591731-36591897 | Rare:65 | ||||
| chr17:36594075-36594265 | Rare:29 | ||||
| chr17:36601488-36601630 | Rare:45 | ||||
| chr17:37406799-37406929 | Rare:52 | ||||
| chr17:37489704-37489907 | Rare:81 | ||||
| chr17:37643312-37643636 | Common:5; Rare:112 | ||||
| chr17:37744651-37744743 | Rare:40; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr17:37745003-37745389 | Rare:92; Clinvar (benign):2 |