| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7313403-7313592 | Common:1; Rare:84 | ||||
| chr17:7351632-7351738 | Rare:19 | ||||
| chr17:7352041-7352212 | Rare:58 | ||||
| chr17:7479517-7479730 | Common:1; Rare:37 | ||||
| chr17:7484215-7484391 | Common:2; Rare:77 | ||||
| chr17:7484505-7484656 | Common:2; Rare:49 | ||||
| chr17:7484690-7484852 | Rare:64 | ||||
| chr17:7503395-7503688 | Rare:81 | ||||
| chr17:7548970-7549222 | Common:2; Rare:56; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:7558528-7558783 | Rare:51 | ||||
| chr17:7561803-7562017 | Common:2; Rare:58 | ||||
| chr17:7577245-7577487 | Rare:57 | ||||
| chr17:7583510-7583865 | Common:1; Rare:141; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr17:7584068-7584196 | Rare:30 | ||||
| chr17:7627531-7627704 | Rare:60 |