| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:75526272-75526525 | Common:1; Rare:52 | ||||
| chr17:75633925-75634139 | Common:2; Rare:50 | ||||
| chr17:75645576-75645885 | Common:3; Rare:64 | ||||
| chr17:75646073-75646670 | Common:6; Rare:126 | ||||
| chr17:75667073-75667448 | Common:5; Rare:123 | ||||
| chr17:75667587-75667726 | Common:1; Rare:41 | ||||
| chr17:75667772-75667791 | Rare:2 | ||||
| chr17:75720989-75721120 | Common:3; Rare:28 | ||||
| chr17:75721147-75721589 | Common:4; Rare:136; Clinvar:2 | ||||
| chr17:75764682-75764730 | Rare:9 | ||||
| chr17:75765056-75765324 | Common:2; Rare:79; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr17:75779288-75779554 | Common:1; Rare:133 | ||||
| chr17:75779728-75780152 | Common:2; Rare:160 | ||||
| chr17:75784246-75784361 | Rare:23 | ||||
| chr17:75784501-75784894 | Common:2; Rare:178 |