| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:78782255-78782572 | Common:9; Rare:105 | ||||
| chr17:78840748-78841114 | Common:2; Rare:137 | ||||
| chr17:78979866-78979999 | Common:1; Rare:26 | ||||
| chr17:80035861-80036004 | Common:1; Rare:50 | ||||
| chr17:80036576-80036663 | Common:2; Rare:24; Clinvar (benign):2 | ||||
| chr17:80147126-80147374 | Common:6; Rare:95 | ||||
| chr17:80220309-80220468 | Common:1; Rare:61; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr17:80415069-80415189 | Common:1; Rare:77 | ||||
| chr17:80415387-80415492 | Common:4; Rare:40 | ||||
| chr17:81295266-81295398 | Common:1; Rare:26 | ||||
| chr17:81512230-81512608 | Common:4; Rare:184; Clinvar:2; Clinvar (benign):12 | ||||
| chr17:81636916-81637246 | Common:3; Rare:129 | ||||
| chr17:81666561-81666763 | Common:1; Rare:89 | ||||
| chr17:81683670-81684052 | Common:4; Rare:196 | ||||
| chr17:81703267-81703530 | Common:2; Rare:81; Clinvar (benign):2 |