| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:28598863-28599181 | Common:9; Rare:275 | ||||
| chr17:28645028-28645403 | Common:3; Rare:416 | ||||
| chr17:28661859-28661980 | Rare:87 | ||||
| chr17:28662065-28662332 | Rare:265 | ||||
| chr17:28674230-28674810 | Common:1; Rare:211 | ||||
| chr17:28710462-28710652 | Common:8; Rare:54 | ||||
| chr17:28710895-28711531 | Common:6; Rare:291 | ||||
| chr17:28719636-28720109 | Common:2; Rare:323 | ||||
| chr17:28720422-28720822 | Common:2; Rare:190 | ||||
| chr17:28725528-28726478 | Common:16; Rare:508 | ||||
| chr17:28726402-28726806 | Common:5; Rare:211 | ||||
| chr17:28726860-28727350 | Common:4; Rare:182 | ||||
| chr17:28727925-28728071 | Rare:35 | ||||
| chr17:28728507-28729252 | Common:6; Rare:430; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr17:28743301-28743694 | Rare:102 |