| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:39200015-39200358 | Common:2; Rare:109 | ||||
| chr17:39451242-39451409 | Common:2; Rare:61 | ||||
| chr17:39688022-39688094 | Rare:22 | ||||
| chr17:40015150-40015441 | Common:1; Rare:59 | ||||
| chr17:40054385-40054565 | Common:1; Rare:40 | ||||
| chr17:40140127-40140569 | Common:5; Rare:202 | ||||
| chr17:40140709-40140773 | Rare:33 | ||||
| chr17:40318033-40318313 | Common:1; Rare:60 | ||||
| chr17:40342037-40342195 | Common:1; Rare:31 | ||||
| chr17:41812620-41813034 | Common:3; Rare:92; Clinvar:5 | ||||
| chr17:41818186-41818422 | Common:1; Rare:91; Clinvar:5; Clinvar (benign):2 | ||||
| chr17:41966547-41966885 | Common:2; Rare:112 | ||||
| chr17:42017139-42017541 | Common:1; Rare:132 | ||||
| chr17:42017548-42017630 | Rare:27 | ||||
| chr17:42154930-42155265 | Common:3; Rare:91 |