| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:68259139-68259231 | Rare:39 | ||||
| chr17:68511609-68511777 | Common:4; Rare:46 | ||||
| chr17:68511823-68512113 | Common:1; Rare:69 | ||||
| chr17:68512292-68512548 | Common:1; Rare:91; Clinvar:2; Clinvar (benign):3 | ||||
| chr17:69327091-69327336 | Common:2; Rare:81 | ||||
| chr17:69414627-69414772 | Rare:31 | ||||
| chr17:72120793-72121034 | Rare:63 | ||||
| chr17:73192809-73193067 | Common:15; Rare:104; Clinvar:2; Clinvar (benign):1 | ||||
| chr17:73232100-73232722 | Common:4; Rare:237 | ||||
| chr17:73311979-73312157 | Rare:45 | ||||
| chr17:74213337-74213532 | Common:4; Rare:41 | ||||
| chr17:74431285-74431416 | Rare:32 | ||||
| chr17:74432012-74432141 | Common:1; Rare:57 | ||||
| chr17:74776111-74776540 | Common:4; Rare:127 | ||||
| chr17:74972684-74972865 | Common:2; Rare:47 |