| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:76072320-76072579 | Common:6; Rare:141 | ||||
| chr17:76103708-76103867 | Common:4; Rare:52 | ||||
| chr17:76265152-76265491 | Common:2; Rare:116 | ||||
| chr17:76353612-76353671 | Rare:24 | ||||
| chr17:76585774-76586104 | Common:5; Rare:82 | ||||
| chr17:76726449-76726914 | Common:5; Rare:180 | ||||
| chr17:76737240-76737687 | Common:5; Rare:189 | ||||
| chr17:77319398-77319654 | Common:3; Rare:69; Clinvar:1; Clinvar (benign):3 | ||||
| chr17:78187045-78187386 | Common:3; Rare:109 | ||||
| chr17:78782219-78782572 | Common:9; Rare:116 | ||||
| chr17:78840740-78841114 | Common:2; Rare:141 | ||||
| chr17:80035855-80036030 | Common:1; Rare:61 | ||||
| chr17:80147075-80147360 | Common:5; Rare:114 | ||||
| chr17:80220309-80220474 | Common:1; Rare:62; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr17:80353853-80354120 | Common:3; Rare:84 |