| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:31442767-31443059 | Common:1; Rare:47 | ||||
| chr16:31458154-31458311 | Common:1; Rare:39 | ||||
| chr16:31458902-31459182 | Rare:82 | ||||
| chr16:31459290-31459517 | Common:1; Rare:94 | ||||
| chr16:31471984-31472188 | Rare:48 | ||||
| chr16:31508351-31508484 | Common:2; Rare:57 | ||||
| chr16:46689130-46689384 | Common:1; Rare:90; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:46689504-46689708 | Common:2; Rare:83; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:46973528-46973768 | Rare:94 | ||||
| chr16:47460917-47461374 | Common:2; Rare:185; Clinvar (benign):2 | ||||
| chr16:48244254-48244601 | Common:2; Rare:103 | ||||
| chr16:50266527-50266573 | Rare:4 | ||||
| chr16:50681306-50681360 | Rare:12 | ||||
| chr16:50693515-50693631 | Rare:46 | ||||
| chr16:50741674-50742209 | Common:7; Rare:169; Clinvar:1 |