| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:40219178-40219402 | Common:2; Rare:77 | ||||
| chr17:40342067-40342183 | Common:1; Rare:21 | ||||
| chr17:40417909-40418214 | Rare:104 | ||||
| chr17:41688631-41688910 | Common:1; Rare:92 | ||||
| chr17:41689328-41689589 | Common:1; Rare:94 | ||||
| chr17:41786696-41787041 | Common:2; Rare:79 | ||||
| chr17:41812724-41813010 | Rare:68; Clinvar:5 | ||||
| chr17:41865345-41865549 | Rare:81 | ||||
| chr17:41918927-41919251 | Common:1; Rare:122 | ||||
| chr17:42017143-42017216 | Rare:13 | ||||
| chr17:42017364-42017492 | Rare:56 | ||||
| chr17:42154943-42155223 | Common:3; Rare:67 | ||||
| chr17:42458730-42458945 | Common:3; Rare:80 | ||||
| chr17:42577680-42577815 | Rare:62 | ||||
| chr17:42609328-42609723 | Common:8; Rare:167; Clinvar (benign):2 |