| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:17823401-17824484 | Common:41; Rare:1265 | ||||
| chr17:17836710-17837214 | Common:11; Rare:245 | ||||
| chr17:17848953-17849475 | Common:8; Rare:149 | ||||
| chr17:17972151-17972970 | Common:15; Rare:966 | ||||
| chr17:18025581-18026688 | Common:5; Rare:250; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:18039077-18039526 | Common:32; Rare:635; Clinvar:2; Clinvar (benign):6 | ||||
| chr17:18039550-18039890 | Rare:95 | ||||
| chr17:18039805-18040495 | Common:1; Rare:141 | ||||
| chr17:18087664-18088064 | Rare:449 | ||||
| chr17:18153840-18154095 | Common:6; Rare:93; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr17:18158039-18158439 | Common:4; Rare:232 | ||||
| chr17:18182254-18182654 | Common:1; Rare:104 | ||||
| chr17:18182790-18183140 | Common:5; Rare:352 | ||||
| chr17:18183202-18183938 | Common:2; Rare:912 | ||||
| chr17:18183924-18184816 | Common:3; Rare:619 |