| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:5486156-5486419 | Common:4; Rare:110 | ||||
| chr17:5772049-5772239 | Common:4; Rare:49 | ||||
| chr17:6077944-6077997 | Rare:15 | ||||
| chr17:6444171-6444478 | Common:2; Rare:97 | ||||
| chr17:6640646-6641089 | Common:7; Rare:138 | ||||
| chr17:6651557-6651640 | Common:1; Rare:32 | ||||
| chr17:7012317-7012677 | Rare:126 | ||||
| chr17:7234465-7234650 | Common:2; Rare:101 | ||||
| chr17:7251946-7252362 | Common:2; Rare:160 | ||||
| chr17:7315112-7315411 | Common:4; Rare:106 | ||||
| chr17:7444872-7445123 | Rare:59; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:7484215-7484370 | Common:1; Rare:61 | ||||
| chr17:7583550-7583874 | Common:1; Rare:131; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr17:7584080-7584099 | Rare:3 | ||||
| chr17:7687468-7687593 | Rare:28 |