| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:37745046-37745200 | Rare:38; Clinvar (benign):2 | ||||
| chr17:38297124-38297231 | Common:3; Rare:52 | ||||
| chr17:38799505-38799652 | Common:2; Rare:38 | ||||
| chr17:38825287-38825427 | Common:1; Rare:43 | ||||
| chr17:38853691-38853895 | Common:3; Rare:82 | ||||
| chr17:39197664-39197981 | Common:2; Rare:72 | ||||
| chr17:39451250-39451403 | Common:2; Rare:54 | ||||
| chr17:39637024-39637165 | Common:2; Rare:40 | ||||
| chr17:39688022-39688176 | Rare:45 | ||||
| chr17:39738227-39738369 | Rare:36 | ||||
| chr17:39927539-39927745 | Common:2; Rare:60 | ||||
| chr17:40054385-40054583 | Common:2; Rare:45 | ||||
| chr17:40140185-40140544 | Common:5; Rare:178 | ||||
| chr17:40417864-40418205 | Rare:106 | ||||
| chr17:41528212-41528513 | Common:1; Rare:77; Clinvar:1 |