| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:40331822-40331996 | Rare:35 | ||||
| chr17:40364659-40364776 | Rare:19 | ||||
| chr17:40445381-40445440 | Rare:9 | ||||
| chr17:40557453-40557716 | Common:1; Rare:40 | ||||
| chr17:41983569-41983783 | Rare:42 | ||||
| chr17:42248707-42248885 | Common:1; Rare:38 | ||||
| chr17:42422733-42422888 | Rare:62; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr17:43166394-43166588 | Common:1; Rare:38 | ||||
| chr17:43315647-43315916 | Common:6; Rare:114 | ||||
| chr17:43368082-43368367 | Common:9; Rare:111 | ||||
| chr17:43388295-43388436 | Rare:28 | ||||
| chr17:43858478-43858628 | Rare:21 | ||||
| chr17:44207697-44207914 | Rare:65 | ||||
| chr17:44215056-44215266 | Common:2; Rare:48 | ||||
| chr17:44325379-44325471 | Common:1; Rare:16 |