| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:77320067-77320329 | Common:1; Rare:67; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr17:78187046-78187391 | Common:3; Rare:114 | ||||
| chr17:78782216-78782545 | Common:5; Rare:97 | ||||
| chr17:78840740-78841055 | Common:2; Rare:114 | ||||
| chr17:80035843-80036031 | Common:1; Rare:66 | ||||
| chr17:80147075-80147215 | Common:4; Rare:77 | ||||
| chr17:80220320-80220468 | Common:1; Rare:56; Clinvar:1 | ||||
| chr17:80337376-80337563 | Common:1; Rare:50 | ||||
| chr17:80375650-80375831 | Common:1; Rare:44 | ||||
| chr17:80384854-80385080 | Rare:50 | ||||
| chr17:80415101-80415509 | Common:5; Rare:203 | ||||
| chr17:81034862-81035175 | Common:2; Rare:126 | ||||
| chr17:81057506-81057797 | Common:3; Rare:61 | ||||
| chr17:81128802-81129152 | Common:1; Rare:82 | ||||
| chr17:81239048-81239321 | Common:2; Rare:90 |