| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:90019755-90019864 | Rare:37 | ||||
| chr16:90019874-90020151 | Common:2; Rare:80 | ||||
| chr16:90022581-90022711 | Rare:52 | ||||
| chr17:714776-714899 | Common:2; Rare:40 | ||||
| chr17:752146-752347 | Common:2; Rare:78 | ||||
| chr17:996753-997054 | Common:1; Rare:77 | ||||
| chr17:1078942-1079039 | Rare:37 | ||||
| chr17:1079120-1079165 | Rare:10 | ||||
| chr17:1400046-1400356 | Common:3; Rare:126 | ||||
| chr17:1516557-1516984 | Common:3; Rare:153 | ||||
| chr17:1684790-1685008 | Common:1; Rare:72; Clinvar:5; Clinvar (benign):1 | ||||
| chr17:1716241-1716544 | Common:3; Rare:89 | ||||
| chr17:1829786-1830038 | Common:6; Rare:108 | ||||
| chr17:2303697-2304001 | Common:2; Rare:116 | ||||
| chr17:2336423-2336572 | Rare:60 |