| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:1829733-1830106 | Common:9; Rare:153 | ||||
| chr17:2030126-2030228 | Rare:53; Clinvar (pathogenic):1 | ||||
| chr17:2030625-2030823 | Rare:39 | ||||
| chr17:2041805-2042143 | Common:6; Rare:161 | ||||
| chr17:2055069-2055145 | Rare:21 | ||||
| chr17:2303298-2303882 | Common:1; Rare:212 | ||||
| chr17:2303885-2304126 | Common:2; Rare:65 | ||||
| chr17:2304199-2304265 | Common:1; Rare:13 | ||||
| chr17:2335870-2336011 | Rare:36 | ||||
| chr17:2336398-2336655 | Rare:102 | ||||
| chr17:2337363-2337569 | Rare:58 | ||||
| chr17:2337932-2338041 | Common:2; Rare:23 | ||||
| chr17:2392611-2393056 | Common:8; Rare:197 | ||||
| chr17:2393179-2393357 | Rare:70 | ||||
| chr17:2393445-2393667 | Common:4; Rare:63 |