| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:39461358-39461600 | Common:1; Rare:66 | ||||
| chr17:39461732-39461933 | Rare:44 | ||||
| chr17:39636966-39637256 | Common:4; Rare:95 | ||||
| chr17:39637281-39637377 | Common:1; Rare:40 | ||||
| chr17:39668492-39668562 | Rare:27 | ||||
| chr17:39687769-39687977 | Rare:90; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr17:39687978-39688224 | Rare:75 | ||||
| chr17:39699869-39700082 | Rare:45 | ||||
| chr17:39730394-39730636 | Common:1; Rare:83 | ||||
| chr17:39738125-39738359 | Common:1; Rare:53 | ||||
| chr17:39927502-39927796 | Common:2; Rare:93 | ||||
| chr17:39980381-39980940 | Common:2; Rare:138 | ||||
| chr17:40054291-40054658 | Common:2; Rare:82 | ||||
| chr17:40054675-40054729 | Rare:12 | ||||
| chr17:40068825-40069030 | Rare:41 |