| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7590073-7590361 | Rare:55 | ||||
| chr17:7627799-7627975 | Common:2; Rare:57 | ||||
| chr17:7650637-7650931 | Common:2; Rare:81 | ||||
| chr17:7674907-7675159 | Rare:77; Clinvar:23; Clinvar (benign):21; Clinvar (pathogenic):13 | ||||
| chr17:7687422-7687697 | Rare:59; Clinvar:2 | ||||
| chr17:7857100-7857314 | Common:1; Rare:110 | ||||
| chr17:7857449-7857741 | Common:2; Rare:95 | ||||
| chr17:7931906-7932257 | Common:5; Rare:96 | ||||
| chr17:8162936-8163072 | Rare:39 | ||||
| chr17:8176343-8176492 | Rare:45 | ||||
| chr17:8210541-8210712 | Common:2; Rare:34 | ||||
| chr17:8248038-8248192 | Common:3; Rare:63; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:8249024-8249338 | Common:1; Rare:70 | ||||
| chr17:8376619-8376806 | Common:1; Rare:84 | ||||
| chr17:8435706-8435970 | Common:3; Rare:108 |