| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:15563447-15563776 | Common:1; Rare:109 | ||||
| chr17:15699630-15699773 | Common:1; Rare:42 | ||||
| chr17:15944967-15945324 | Common:3; Rare:93 | ||||
| chr17:15999598-16000032 | Common:3; Rare:186; Clinvar:6; Clinvar (benign):12; Clinvar (pathogenic):2 | ||||
| chr17:16039590-16039806 | Common:1; Rare:52 | ||||
| chr17:16040440-16040730 | Common:2; Rare:53 | ||||
| chr17:16215532-16215632 | Rare:46 | ||||
| chr17:16217080-16217240 | Rare:43; Clinvar:1 | ||||
| chr17:17496392-17496566 | Rare:45 | ||||
| chr17:17591595-17591932 | Common:1; Rare:96 | ||||
| chr17:17823564-17823869 | Common:5; Rare:139 | ||||
| chr17:18039018-18039385 | Common:3; Rare:94; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:18039765-18039801 | Rare:9 | ||||
| chr17:18087771-18088009 | Rare:67 | ||||
| chr17:18225374-18225702 | Common:4; Rare:109 |