| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:42745023-42745172 | Common:3; Rare:54 | ||||
| chr17:42760737-42760903 | Common:4; Rare:51 | ||||
| chr17:42760963-42761270 | Rare:79 | ||||
| chr17:42773333-42773475 | Rare:40 | ||||
| chr17:42798643-42798785 | Rare:46 | ||||
| chr17:42833340-42833471 | Rare:50 | ||||
| chr17:42964409-42964536 | Rare:60 | ||||
| chr17:42980453-42980571 | Common:1; Rare:43 | ||||
| chr17:42998368-42998541 | Common:4; Rare:52 | ||||
| chr17:43025119-43025363 | Rare:62 | ||||
| chr17:43125344-43125601 | Rare:53; Clinvar:3; Clinvar (benign):2 | ||||
| chr17:43170191-43170523 | Common:2; Rare:72 | ||||
| chr17:43170972-43171267 | Common:1; Rare:99 | ||||
| chr17:43398872-43399006 | Common:1; Rare:41 | ||||
| chr17:43483651-43484038 | Rare:104 |