| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7575296-7575592 | Rare:108 | ||||
| chr17:7576573-7576826 | Common:1; Rare:76 | ||||
| chr17:7579104-7579404 | Common:1; Rare:111 | ||||
| chr17:7579409-7579728 | Common:1; Rare:104 | ||||
| chr17:7583109-7583154 | Rare:14 | ||||
| chr17:7583467-7583955 | Common:1; Rare:186; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr17:7583987-7584205 | Rare:58 | ||||
| chr17:7590071-7590278 | Rare:40 | ||||
| chr17:7613786-7613831 | Rare:7 | ||||
| chr17:7614034-7614303 | Rare:81 | ||||
| chr17:7614452-7614509 | Rare:6 | ||||
| chr17:7614521-7614701 | Rare:40 | ||||
| chr17:7614715-7615404 | Rare:202 | ||||
| chr17:7627389-7627472 | Rare:25 | ||||
| chr17:7627551-7627652 | Rare:31 |