| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:74466440-74466692 | Rare:62 | ||||
| chr17:74748392-74748635 | Common:2; Rare:83 | ||||
| chr17:74776329-74776506 | Common:4; Rare:50 | ||||
| chr17:75109878-75109977 | Common:1; Rare:23 | ||||
| chr17:75130788-75131099 | Common:2; Rare:110 | ||||
| chr17:75205390-75205734 | Rare:99 | ||||
| chr17:75261590-75261931 | Common:4; Rare:107; Clinvar (benign):2 | ||||
| chr17:75289387-75289628 | Common:1; Rare:75; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:75667127-75667396 | Common:4; Rare:93 | ||||
| chr17:75784556-75784872 | Common:2; Rare:140 | ||||
| chr17:75904879-75905035 | Common:2; Rare:53 | ||||
| chr17:75979121-75979283 | Rare:42; Clinvar:4 | ||||
| chr17:75979393-75979470 | Rare:21 | ||||
| chr17:76103696-76103886 | Common:6; Rare:66 | ||||
| chr17:76141243-76141419 | Common:1; Rare:48 |