| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7352088-7352196 | Rare:32 | ||||
| chr17:7479496-7479740 | Common:1; Rare:44 | ||||
| chr17:7484215-7484371 | Common:1; Rare:62 | ||||
| chr17:7580210-7580515 | Common:1; Rare:90 | ||||
| chr17:7583535-7583865 | Common:1; Rare:133; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr17:7614867-7614938 | Rare:26 | ||||
| chr17:7627656-7627762 | Rare:44 | ||||
| chr17:7687476-7687660 | Rare:39 | ||||
| chr17:7857467-7858003 | Common:4; Rare:174 | ||||
| chr17:7931910-7932235 | Common:5; Rare:87 | ||||
| chr17:8152359-8152567 | Common:2; Rare:50 | ||||
| chr17:8176354-8176492 | Rare:41 | ||||
| chr17:8248029-8248162 | Common:3; Rare:61; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:8965674-8965766 | Common:1; Rare:25 | ||||
| chr17:10697417-10697660 | Common:4; Rare:107; Clinvar:5; Clinvar (benign):5 |