| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:77146014-77146608 | Common:2; Rare:123 | ||||
| chr17:77146978-77147176 | Common:3; Rare:51 | ||||
| chr17:77147705-77147785 | Common:1; Rare:16 | ||||
| chr17:77148789-77148876 | Rare:24 | ||||
| chr17:77149588-77149867 | Common:1; Rare:52 | ||||
| chr17:77152560-77152813 | Common:2; Rare:57 | ||||
| chr17:77154294-77154620 | Common:4; Rare:60 | ||||
| chr17:77164636-77164757 | Rare:16 | ||||
| chr17:77169198-77169475 | Common:3; Rare:54 | ||||
| chr17:77175318-77175371 | Common:1; Rare:11 | ||||
| chr17:77219456-77219520 | Rare:7 | ||||
| chr17:77390173-77390298 | Rare:25 | ||||
| chr17:77492676-77493013 | Common:2; Rare:76; Clinvar (benign):2 | ||||
| chr17:77958440-77958715 | Common:2; Rare:94 | ||||
| chr17:78381677-78381731 | Rare:11 |