| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:31202548-31202971 | Common:2; Rare:145 | ||||
| chr16:31442771-31443059 | Common:1; Rare:47 | ||||
| chr16:31458230-31458328 | Rare:28 | ||||
| chr16:31459091-31459188 | Rare:31 | ||||
| chr16:31459263-31459517 | Common:1; Rare:107 | ||||
| chr16:31471984-31472183 | Rare:46 | ||||
| chr16:31508192-31508508 | Common:5; Rare:141 | ||||
| chr16:46689475-46689669 | Common:1; Rare:65; Clinvar (benign):1 | ||||
| chr16:46973555-46973757 | Rare:85 | ||||
| chr16:47460986-47461408 | Common:3; Rare:169; Clinvar (benign):3 | ||||
| chr16:48244210-48244606 | Common:2; Rare:118 | ||||
| chr16:50693520-50693651 | Rare:53 | ||||
| chr16:53434659-53434734 | Common:1; Rare:28 | ||||
| chr16:53703817-53704213 | Common:1; Rare:124; Clinvar:4; Clinvar (benign):2 | ||||
| chr16:54285748-54285961 | Rare:80 |