| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:16039590-16039709 | Common:1; Rare:32 | ||||
| chr17:16215504-16215657 | Common:1; Rare:62 | ||||
| chr17:17496388-17496575 | Common:2; Rare:51 | ||||
| chr17:17591587-17591926 | Common:2; Rare:96 | ||||
| chr17:17823590-17823780 | Common:5; Rare:90 | ||||
| chr17:18039145-18039381 | Common:3; Rare:60; Clinvar (benign):1 | ||||
| chr17:18039602-18039674 | Rare:27 | ||||
| chr17:18183046-18183111 | Rare:24 | ||||
| chr17:18183207-18183487 | Rare:68 | ||||
| chr17:18183794-18183942 | Rare:64 | ||||
| chr17:18184470-18184610 | Rare:43 | ||||
| chr17:18184736-18185020 | Common:1; Rare:61 | ||||
| chr17:18225355-18225661 | Common:3; Rare:98 | ||||
| chr17:18253319-18253669 | Rare:126 | ||||
| chr17:18254524-18254824 | Rare:103 |