| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:43006959-43007078 | Rare:32 | ||||
| chr17:43021996-43022186 | Common:2; Rare:67 | ||||
| chr17:43022292-43022510 | Rare:65 | ||||
| chr17:43024515-43024628 | Rare:10 | ||||
| chr17:43025043-43025275 | Rare:50 | ||||
| chr17:43125028-43125119 | Rare:21; Clinvar (benign):1 | ||||
| chr17:43125233-43125748 | Rare:136; Clinvar:7; Clinvar (benign):10 | ||||
| chr17:43169807-43170078 | Common:4; Rare:44 | ||||
| chr17:43170121-43170565 | Common:3; Rare:96 | ||||
| chr17:43170903-43171353 | Common:1; Rare:147 | ||||
| chr17:43211694-43211915 | Common:2; Rare:52 | ||||
| chr17:43398888-43399031 | Common:2; Rare:47 | ||||
| chr17:43483571-43484073 | Rare:135 | ||||
| chr17:43545377-43545544 | Rare:42 | ||||
| chr17:43545590-43545847 | Common:2; Rare:69 |