| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:8231356-8231648 | Rare:75; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr17:8248025-8248184 | Common:3; Rare:68; Clinvar:3; Clinvar (benign):2 | ||||
| chr17:8249024-8249325 | Common:1; Rare:67 | ||||
| chr17:8295334-8295532 | Common:1; Rare:50 | ||||
| chr17:8412998-8413262 | Common:3; Rare:48 | ||||
| chr17:8435647-8436024 | Common:5; Rare:151 | ||||
| chr17:8867633-8867775 | Common:1; Rare:27 | ||||
| chr17:8965621-8965919 | Common:2; Rare:72 | ||||
| chr17:10019831-10020093 | Common:1; Rare:66 | ||||
| chr17:10198407-10198486 | Rare:13 | ||||
| chr17:10198639-10199002 | Common:3; Rare:114 | ||||
| chr17:10697468-10697660 | Common:4; Rare:89; Clinvar:5; Clinvar (benign):3 | ||||
| chr17:10729980-10730099 | Common:3; Rare:28 | ||||
| chr17:11997345-11997631 | Common:3; Rare:111 | ||||
| chr17:13017935-13018260 | Common:5; Rare:96; Clinvar (benign):2 |