| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:40642453-40642744 | Rare:51; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:40646494-40646750 | Rare:42 | ||||
| chr17:40819728-40819754 | Rare:10 | ||||
| chr17:40942500-40942713 | Common:4; Rare:32 | ||||
| chr17:41758346-41758726 | Common:1; Rare:96; Clinvar:11; Clinvar (benign):5 | ||||
| chr17:41769134-41769426 | Common:1; Rare:92; Clinvar:10; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr17:41777932-41778152 | Common:2; Rare:43 | ||||
| chr17:41868698-41869167 | Common:2; Rare:96 | ||||
| chr17:41877160-41877432 | Common:1; Rare:45 | ||||
| chr17:41894681-41894952 | Common:2; Rare:38 | ||||
| chr17:41911267-41911368 | Rare:19 | ||||
| chr17:41985073-41985355 | Rare:60 | ||||
| chr17:42127456-42127508 | Rare:7 | ||||
| chr17:42192723-42193024 | Rare:80 | ||||
| chr17:42222551-42222838 | Common:2; Rare:52 |