| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:40418366-40418508 | Rare:24 | ||||
| chr17:40443190-40443299 | Rare:25 | ||||
| chr17:40443301-40443504 | Common:1; Rare:66 | ||||
| chr17:40443738-40443895 | Common:1; Rare:45 | ||||
| chr17:40560403-40560548 | Rare:35 | ||||
| chr17:40647336-40647432 | Rare:25 | ||||
| chr17:40647749-40647861 | Rare:31 | ||||
| chr17:40648013-40648209 | Rare:52 | ||||
| chr17:40648218-40648359 | Common:1; Rare:32 | ||||
| chr17:40648364-40648459 | Common:1; Rare:21 | ||||
| chr17:40648516-40648687 | Rare:27 | ||||
| chr17:40648713-40648824 | Rare:12 | ||||
| chr17:40818796-40819201 | Common:13; Rare:269; Clinvar (benign):2 | ||||
| chr17:40936635-40936940 | Rare:52 | ||||
| chr17:41009114-41009423 | Common:2; Rare:51 |