| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:2025149-2025742 | Rare:171 | ||||
| chr17:2030022-2030239 | Common:1; Rare:90; Clinvar (pathogenic):1 | ||||
| chr17:2030345-2030375 | Common:1; Rare:4 | ||||
| chr17:2030652-2030845 | Rare:40 | ||||
| chr17:2041864-2042159 | Common:6; Rare:142 | ||||
| chr17:2042201-2042301 | Common:1; Rare:32 | ||||
| chr17:2054796-2055149 | Common:1; Rare:103 | ||||
| chr17:2244524-2244673 | Rare:31 | ||||
| chr17:2303091-2303114 | Rare:5 | ||||
| chr17:2303265-2304060 | Common:3; Rare:279 | ||||
| chr17:2304204-2304266 | Common:1; Rare:13 | ||||
| chr17:2335875-2336052 | Rare:51 | ||||
| chr17:2336338-2336657 | Rare:129 | ||||
| chr17:2336958-2337151 | Common:2; Rare:46 | ||||
| chr17:2337213-2337255 | Rare:5 |