| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:75182814-75183216 | Common:2; Rare:138 | ||||
| chr17:75205360-75205749 | Common:1; Rare:126 | ||||
| chr17:75261590-75261963 | Common:4; Rare:125; Clinvar (benign):3 | ||||
| chr17:75289387-75289613 | Common:1; Rare:71; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:75393764-75394056 | Common:1; Rare:65 | ||||
| chr17:75456465-75456641 | Rare:48 | ||||
| chr17:75667131-75667378 | Common:4; Rare:79 | ||||
| chr17:75784558-75784872 | Common:2; Rare:138 | ||||
| chr17:75855299-75855637 | Common:1; Rare:86 | ||||
| chr17:75904878-75905218 | Common:4; Rare:93 | ||||
| chr17:75941023-75941084 | Rare:18 | ||||
| chr17:75979126-75979283 | Rare:40; Clinvar:4 | ||||
| chr17:76072487-76072664 | Rare:54 | ||||
| chr17:76103696-76103876 | Common:5; Rare:64 | ||||
| chr17:76353608-76353976 | Common:2; Rare:129 |