| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:1762840-1763130 | Common:8; Rare:99 | ||||
| chr17:1763170-1763490 | Common:1; Rare:134 | ||||
| chr17:1829239-1829639 | Common:2; Rare:89 | ||||
| chr17:1829708-1830108 | Common:54; Rare:906 | ||||
| chr17:2025227-2025732 | Rare:358 | ||||
| chr17:2029867-2030680 | Common:7; Rare:503; Clinvar (pathogenic):5 | ||||
| chr17:2030639-2031047 | Common:1; Rare:157 | ||||
| chr17:2041390-2041720 | Common:2; Rare:134 | ||||
| chr17:2041749-2042163 | Common:16; Rare:460 | ||||
| chr17:2053531-2053931 | Common:1; Rare:132 | ||||
| chr17:2088830-2089950 | Common:4; Rare:266 | ||||
| chr17:2213850-2214270 | Rare:142 | ||||
| chr17:2214290-2214750 | Common:3; Rare:139 | ||||
| chr17:2302961-2303361 | Rare:90 | ||||
| chr17:2303375-2304100 | Common:15; Rare:1211 |