| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:42682472-42682635 | Common:1; Rare:41 | ||||
| chr17:42760713-42760817 | Common:4; Rare:33 | ||||
| chr17:42761027-42761049 | Rare:8 | ||||
| chr17:42761075-42761276 | Rare:57 | ||||
| chr17:42761325-42761354 | Common:1; Rare:4 | ||||
| chr17:42798643-42798863 | Rare:69 | ||||
| chr17:42833367-42833479 | Rare:43 | ||||
| chr17:42964422-42964536 | Rare:53 | ||||
| chr17:43025120-43025396 | Rare:68 | ||||
| chr17:43125338-43125662 | Rare:80; Clinvar:3; Clinvar (benign):2 | ||||
| chr17:43170292-43170332 | Rare:6 | ||||
| chr17:43171002-43171251 | Rare:80 | ||||
| chr17:43398897-43399014 | Rare:33 | ||||
| chr17:43778907-43779076 | Rare:38 | ||||
| chr17:43833114-43833315 | Common:2; Rare:58 |