| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:69327087-69327364 | Common:2; Rare:90 | ||||
| chr17:70169308-70169539 | Common:1; Rare:65 | ||||
| chr17:72120784-72121047 | Rare:70 | ||||
| chr17:73192841-73193067 | Common:10; Rare:69; Clinvar:2; Clinvar (benign):1 | ||||
| chr17:73232137-73232707 | Common:4; Rare:218 | ||||
| chr17:74776295-74776516 | Common:4; Rare:66 | ||||
| chr17:75012513-75012700 | Common:1; Rare:45 | ||||
| chr17:75109897-75109994 | Common:1; Rare:27 | ||||
| chr17:75131467-75131728 | Common:3; Rare:98 | ||||
| chr17:75182830-75183218 | Common:2; Rare:136 | ||||
| chr17:75205370-75205686 | Common:1; Rare:84 | ||||
| chr17:75261588-75261925 | Common:4; Rare:102; Clinvar (benign):1 | ||||
| chr17:75289387-75289630 | Common:1; Rare:76; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:75393824-75394020 | Common:1; Rare:52 | ||||
| chr17:75456472-75456656 | Rare:48 |