| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:76737325-76737537 | Common:2; Rare:81 | ||||
| chr17:76737877-76738034 | Common:3; Rare:44 | ||||
| chr17:77140672-77141038 | Common:1; Rare:130 | ||||
| chr17:77319474-77319619 | Common:3; Rare:41; Clinvar:1; Clinvar (benign):3 | ||||
| chr17:77450278-77450567 | Common:2; Rare:61 | ||||
| chr17:78168497-78168640 | Rare:43 | ||||
| chr17:78187044-78187410 | Common:3; Rare:126 | ||||
| chr17:78782233-78782554 | Common:9; Rare:105 | ||||
| chr17:78840745-78841099 | Common:2; Rare:134 | ||||
| chr17:78977150-78977271 | Common:3; Rare:26 | ||||
| chr17:80035843-80036016 | Common:1; Rare:61 | ||||
| chr17:80147069-80147360 | Common:5; Rare:116 | ||||
| chr17:80220279-80220459 | Common:1; Rare:73; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr17:80415109-80415492 | Common:5; Rare:193 | ||||
| chr17:81239048-81239317 | Common:2; Rare:89 |