| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:78187012-78187376 | Common:3; Rare:126 | ||||
| chr17:78214072-78214390 | Common:5; Rare:101 | ||||
| chr17:78378531-78378687 | Common:1; Rare:56 | ||||
| chr17:78782229-78782512 | Common:5; Rare:90 | ||||
| chr17:78840736-78841124 | Common:2; Rare:145 | ||||
| chr17:78979910-78980077 | Common:2; Rare:36 | ||||
| chr17:79009732-79009943 | Common:8; Rare:61; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:79777842-79778236 | Common:1; Rare:177 | ||||
| chr17:79993689-79993844 | Common:1; Rare:28 | ||||
| chr17:80035849-80036042 | Common:1; Rare:67 | ||||
| chr17:80036521-80036668 | Common:2; Rare:38; Clinvar (benign):2 | ||||
| chr17:80146999-80147331 | Common:8; Rare:139 | ||||
| chr17:80220309-80220469 | Common:1; Rare:62; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr17:80415105-80415189 | Common:1; Rare:56 | ||||
| chr17:80544771-80544902 | Rare:29 |