| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:37744873-37745392 | Common:2; Rare:141; Clinvar:2; Clinvar (benign):4 | ||||
| chr17:38705111-38705334 | Common:1; Rare:59 | ||||
| chr17:38724430-38724685 | Common:1; Rare:42 | ||||
| chr17:38725415-38725715 | Common:1; Rare:78 | ||||
| chr17:38730044-38730413 | Rare:99 | ||||
| chr17:38730813-38731026 | Common:1; Rare:42 | ||||
| chr17:38749770-38749922 | Rare:34 | ||||
| chr17:38752465-38752829 | Common:4; Rare:96 | ||||
| chr17:38825268-38825405 | Common:2; Rare:41 | ||||
| chr17:38853685-38853895 | Common:3; Rare:83 | ||||
| chr17:38869944-38870258 | Common:2; Rare:84 | ||||
| chr17:39200036-39200352 | Common:2; Rare:101 | ||||
| chr17:39401614-39401819 | Common:1; Rare:56 | ||||
| chr17:39451250-39451403 | Common:2; Rare:54 | ||||
| chr17:39462360-39462579 | Rare:64 |