| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:43778894-43779308 | Common:3; Rare:104 | ||||
| chr17:43833101-43833317 | Common:2; Rare:62 | ||||
| chr17:43900596-43900766 | Rare:53 | ||||
| chr17:43907490-43907608 | Rare:43 | ||||
| chr17:44070570-44070947 | Common:3; Rare:126; Clinvar:4; Clinvar (benign):2 | ||||
| chr17:44123639-44123884 | Common:3; Rare:64 | ||||
| chr17:44186653-44187026 | Common:1; Rare:133 | ||||
| chr17:44187161-44187274 | Rare:31 | ||||
| chr17:44220825-44220989 | Rare:48 | ||||
| chr17:44221208-44221427 | Rare:62 | ||||
| chr17:44222069-44222321 | Rare:54 | ||||
| chr17:44308425-44308835 | Common:2; Rare:119 | ||||
| chr17:44324771-44325010 | Common:2; Rare:85 | ||||
| chr17:44503366-44503727 | Rare:137 | ||||
| chr17:44758907-44759208 | Common:2; Rare:77 |