| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7350142-7350426 | Common:2; Rare:87 | ||||
| chr17:7351619-7351738 | Rare:22 | ||||
| chr17:7352033-7352206 | Rare:59 | ||||
| chr17:7355023-7355173 | Common:1; Rare:19 | ||||
| chr17:7420204-7420672 | Common:2; Rare:141 | ||||
| chr17:7425484-7425615 | Common:1; Rare:26 | ||||
| chr17:7479496-7479709 | Common:1; Rare:36 | ||||
| chr17:7481417-7481499 | Rare:21 | ||||
| chr17:7483922-7484002 | Common:2; Rare:18 | ||||
| chr17:7484214-7484381 | Common:1; Rare:69 | ||||
| chr17:7484653-7484852 | Rare:86 | ||||
| chr17:7497810-7498154 | Common:3; Rare:132 | ||||
| chr17:7548993-7549237 | Common:3; Rare:56; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:7558067-7558286 | Common:1; Rare:39 | ||||
| chr17:7558712-7559020 | Common:1; Rare:61 |