| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:40648392-40648459 | Rare:17 | ||||
| chr17:40648551-40648737 | Rare:28 | ||||
| chr17:40818787-40819199 | Common:13; Rare:271; Clinvar (benign):2 | ||||
| chr17:40819615-40819689 | Rare:21 | ||||
| chr17:41688592-41688986 | Common:1; Rare:160 | ||||
| chr17:41689214-41689626 | Common:4; Rare:149 | ||||
| chr17:41689894-41690198 | Rare:78 | ||||
| chr17:41811626-41811796 | Rare:50 | ||||
| chr17:41811928-41812091 | Rare:62 | ||||
| chr17:41812884-41813010 | Rare:33 | ||||
| chr17:41836169-41836372 | Common:2; Rare:53 | ||||
| chr17:41864836-41864944 | Rare:24 | ||||
| chr17:41865112-41865157 | Rare:9 | ||||
| chr17:41865278-41865581 | Common:2; Rare:138 | ||||
| chr17:41918860-41919285 | Common:2; Rare:152; Clinvar:1 |