| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:48932579-48932836 | Common:3; Rare:36 | ||||
| chr17:48944696-48944909 | Common:2; Rare:72 | ||||
| chr17:48996975-48997512 | Rare:117 | ||||
| chr17:48998004-48998366 | Common:2; Rare:109 | ||||
| chr17:49414798-49415126 | Common:3; Rare:79 | ||||
| chr17:49707864-49707988 | Rare:64 | ||||
| chr17:49708144-49708306 | Rare:51 | ||||
| chr17:49788590-49788831 | Common:1; Rare:84 | ||||
| chr17:50055682-50056595 | Common:7; Rare:215 | ||||
| chr17:50076321-50076679 | Common:3; Rare:126; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr17:50274310-50274494 | Rare:44 | ||||
| chr17:50345932-50346142 | Common:4; Rare:69 | ||||
| chr17:50355529-50355803 | Common:3; Rare:77 | ||||
| chr17:50372823-50373265 | Common:5; Rare:139 | ||||
| chr17:50397213-50397569 | Common:3; Rare:109 |