| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:42107663-42108063 | Common:4; Rare:403 | ||||
| chr17:42112547-42113101 | Common:17; Rare:274 | ||||
| chr17:42120066-42121800 | Common:11; Rare:942 | ||||
| chr17:42128230-42128590 | Common:2; Rare:78 | ||||
| chr17:42153980-42155284 | Common:16; Rare:785 | ||||
| chr17:42181130-42181800 | Common:8; Rare:310 | ||||
| chr17:42193691-42194091 | Rare:56 | ||||
| chr17:42194344-42194744 | Rare:163 | ||||
| chr17:42275250-42276020 | Common:3; Rare:147 | ||||
| chr17:42276180-42277540 | Common:9; Rare:1123 | ||||
| chr17:42286558-42288623 | Common:8; Rare:1164 | ||||
| chr17:42289053-42290080 | Common:12; Rare:905 | ||||
| chr17:42315975-42317232 | Common:10; Rare:459; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr17:42317210-42317907 | Common:8; Rare:374 | ||||
| chr17:42318027-42318427 | Common:4; Rare:67 |