| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:42422931-42423435 | Common:2; Rare:148; Clinvar:4 | ||||
| chr17:42458738-42458945 | Common:3; Rare:79 | ||||
| chr17:42520173-42520381 | Rare:45 | ||||
| chr17:42577675-42577844 | Rare:82 | ||||
| chr17:42609314-42609767 | Common:8; Rare:186; Clinvar (benign):2 | ||||
| chr17:42682417-42682589 | Rare:41 | ||||
| chr17:42683669-42683984 | Common:2; Rare:75 | ||||
| chr17:42709888-42710138 | Common:3; Rare:47 | ||||
| chr17:42760974-42761049 | Rare:15 | ||||
| chr17:42761056-42761354 | Common:2; Rare:84 | ||||
| chr17:42773375-42773475 | Rare:30 | ||||
| chr17:42798672-42798785 | Rare:36 | ||||
| chr17:42833391-42833497 | Rare:46 | ||||
| chr17:42851052-42851267 | Rare:52 | ||||
| chr17:42852657-42852933 | Common:1; Rare:102 |