| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:2593861-2593970 | Common:1; Rare:34; Clinvar:2; Clinvar (benign):3 | ||||
| chr17:2711762-2712031 | Common:2; Rare:75 | ||||
| chr17:3668571-3668861 | Common:1; Rare:118 | ||||
| chr17:3695375-3695590 | Rare:37 | ||||
| chr17:3723772-3723903 | Common:1; Rare:72 | ||||
| chr17:4143011-4143225 | Rare:71 | ||||
| chr17:4143605-4143735 | Common:4; Rare:76 | ||||
| chr17:4263948-4264072 | Rare:51 | ||||
| chr17:4704116-4704271 | Rare:78 | ||||
| chr17:4806987-4807192 | Common:4; Rare:66 | ||||
| chr17:4939912-4940130 | Common:2; Rare:74 | ||||
| chr17:4950382-4950583 | Rare:51 | ||||
| chr17:5123102-5123404 | Rare:101 | ||||
| chr17:5191838-5192106 | Common:2; Rare:88 | ||||
| chr17:5419625-5420208 | Common:6; Rare:187 |