| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:37609268-37609561 | Common:1; Rare:116 | ||||
| chr17:37745028-37745207 | Rare:44; Clinvar (benign):2 | ||||
| chr17:38428287-38428492 | Common:8; Rare:78 | ||||
| chr17:38705018-38705340 | Common:2; Rare:74 | ||||
| chr17:38706095-38706152 | Rare:27 | ||||
| chr17:38706654-38706974 | Common:2; Rare:72 | ||||
| chr17:38749818-38749922 | Rare:18 | ||||
| chr17:38752501-38752829 | Common:4; Rare:91 | ||||
| chr17:38825191-38825414 | Common:2; Rare:71 | ||||
| chr17:38853429-38853472 | Rare:14 | ||||
| chr17:38853685-38853904 | Common:4; Rare:85 | ||||
| chr17:38869992-38870256 | Common:1; Rare:70 | ||||
| chr17:39199992-39200486 | Common:4; Rare:159 | ||||
| chr17:39200948-39201345 | Common:1; Rare:91 | ||||
| chr17:39401598-39401816 | Common:1; Rare:61 |