| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:74776295-74776499 | Common:4; Rare:61 | ||||
| chr17:75012546-75012692 | Common:1; Rare:37 | ||||
| chr17:75182815-75183216 | Common:2; Rare:138 | ||||
| chr17:75205380-75205720 | Common:1; Rare:98 | ||||
| chr17:75261590-75261925 | Common:4; Rare:102; Clinvar (benign):1 | ||||
| chr17:75271161-75271362 | Common:2; Rare:36 | ||||
| chr17:75393702-75394066 | Common:1; Rare:90 | ||||
| chr17:75667136-75667370 | Common:4; Rare:74 | ||||
| chr17:75784558-75784868 | Common:2; Rare:135 | ||||
| chr17:75904879-75905233 | Common:4; Rare:96 | ||||
| chr17:75941023-75941222 | Common:1; Rare:63 | ||||
| chr17:75979150-75979271 | Rare:31; Clinvar:3 | ||||
| chr17:76072497-76072540 | Rare:21 | ||||
| chr17:76103712-76103876 | Common:4; Rare:53 | ||||
| chr17:76726491-76726911 | Common:5; Rare:159 |