| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7013095-7013252 | Common:1; Rare:40 | ||||
| chr17:7013310-7013436 | Rare:46 | ||||
| chr17:7013507-7013695 | Rare:51 | ||||
| chr17:7014316-7014352 | Rare:10 | ||||
| chr17:7014361-7015192 | Common:13; Rare:280 | ||||
| chr17:7035500-7035623 | Common:1; Rare:26 | ||||
| chr17:7035687-7036574 | Common:3; Rare:229 | ||||
| chr17:7219698-7220013 | Common:3; Rare:115; Clinvar:6; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr17:7220253-7220670 | Common:2; Rare:130; Clinvar:7; Clinvar (benign):1; Clinvar (pathogenic):3 | ||||
| chr17:7234067-7234623 | Rare:233 | ||||
| chr17:7234626-7234715 | Common:1; Rare:33 | ||||
| chr17:7237665-7238033 | Common:1; Rare:104 | ||||
| chr17:7238176-7238375 | Rare:25 | ||||
| chr17:7238678-7238720 | Rare:2 | ||||
| chr17:7238913-7238974 | Rare:14 |