| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:59668538-59668947 | Common:2; Rare:62; Clinvar (pathogenic):1 | ||||
| chr17:59681005-59681404 | Common:1; Rare:87; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr17:59682357-59683007 | Rare:110 | ||||
| chr17:59690344-59690714 | Rare:52 | ||||
| chr17:59693194-59693370 | Rare:26 | ||||
| chr17:59700654-59700661 | Rare:2 | ||||
| chr17:59706387-59706659 | Common:2; Rare:51 | ||||
| chr17:59754625-59754658 | Rare:3 | ||||
| chr17:59756485-59756740 | Common:1; Rare:44 | ||||
| chr17:59763953-59764360 | Common:2; Rare:61 | ||||
| chr17:59767255-59767441 | Rare:20 | ||||
| chr17:59777896-59777916 | Rare:2 | ||||
| chr17:59783435-59783792 | Common:1; Rare:62 | ||||
| chr17:59786497-59786781 | Rare:53 | ||||
| chr17:59829405-59829602 | Common:1; Rare:24 |