| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:31321588-31321770 | Common:3; Rare:29 | ||||
| chr17:32350012-32350234 | Rare:114 | ||||
| chr17:32360839-32360966 | Rare:41 | ||||
| chr17:32444367-32444599 | Rare:95 | ||||
| chr17:34961481-34961575 | Common:1; Rare:43 | ||||
| chr17:34980443-34980796 | Common:5; Rare:113 | ||||
| chr17:34981099-34981178 | Rare:12 | ||||
| chr17:35063673-35063836 | Rare:25 | ||||
| chr17:35242910-35243110 | Rare:69 | ||||
| chr17:35537652-35537723 | Common:1; Rare:10 | ||||
| chr17:35578511-35578684 | Common:1; Rare:45; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:35587222-35587554 | Rare:82 | ||||
| chr17:35795615-35795726 | Rare:27 | ||||
| chr17:36090133-36090204 | Rare:13 | ||||
| chr17:36103584-36103832 | Common:1; Rare:55 |