| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:57867984-57868384 | Common:2; Rare:120 | ||||
| chr17:57954960-57955180 | Common:1; Rare:58 | ||||
| chr17:57955200-57955750 | Common:1; Rare:108 | ||||
| chr17:57987429-57988219 | Common:6; Rare:253 | ||||
| chr17:57988126-57988267 | Rare:44 | ||||
| chr17:57988172-57988587 | Common:26; Rare:548 | ||||
| chr17:58005902-58006730 | Common:10; Rare:653 | ||||
| chr17:58006746-58007146 | Common:2; Rare:90 | ||||
| chr17:58007099-58007471 | Common:7; Rare:869 | ||||
| chr17:58007490-58008010 | Common:5; Rare:366 | ||||
| chr17:58082815-58082984 | Rare:61 | ||||
| chr17:58083113-58083540 | Common:26; Rare:719 | ||||
| chr17:58219087-58219515 | Common:9; Rare:656; Clinvar:31; Clinvar (benign):32; Clinvar (pathogenic):3 | ||||
| chr17:58328279-58329735 | Common:9; Rare:789 | ||||
| chr17:58351980-58352587 | Common:38; Rare:918 |