| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:50194571-50194829 | Common:2; Rare:73; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):4 | ||||
| chr17:50195432-50195669 | Rare:54; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr17:50372894-50372986 | Rare:22 | ||||
| chr17:50532376-50532721 | Common:3; Rare:79 | ||||
| chr17:50707545-50707827 | Common:5; Rare:85 | ||||
| chr17:50707976-50708072 | Rare:18 | ||||
| chr17:50719452-50719667 | Rare:86 | ||||
| chr17:50866335-50866558 | Common:2; Rare:70 | ||||
| chr17:51120757-51120983 | Rare:95 | ||||
| chr17:51153293-51153637 | Common:1; Rare:89 | ||||
| chr17:51166274-51166552 | Common:2; Rare:64 | ||||
| chr17:51260149-51260592 | Common:3; Rare:163 | ||||
| chr17:54968595-54968799 | Common:3; Rare:95 | ||||
| chr17:55722819-55723161 | Common:2; Rare:70 | ||||
| chr17:55751309-55751426 | Common:2; Rare:41 |