| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:31442755-31443059 | Common:1; Rare:50 | ||||
| chr16:31459353-31459510 | Common:1; Rare:64 | ||||
| chr16:31471845-31472186 | Rare:71 | ||||
| chr16:31508374-31508464 | Common:1; Rare:33 | ||||
| chr16:31527694-31528020 | Common:2; Rare:52 | ||||
| chr16:46689134-46689242 | Common:1; Rare:58; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:46689506-46689724 | Common:2; Rare:92; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:46973561-46973781 | Rare:92 | ||||
| chr16:47461012-47461374 | Common:2; Rare:144; Clinvar (benign):2 | ||||
| chr16:48244251-48244621 | Common:2; Rare:107 | ||||
| chr16:48385289-48385528 | Common:3; Rare:96 | ||||
| chr16:50065900-50066001 | Common:2; Rare:37 | ||||
| chr16:50245918-50246178 | Common:2; Rare:61 | ||||
| chr16:50266422-50266573 | Common:1; Rare:42 | ||||
| chr16:50741625-50742204 | Common:7; Rare:181; Clinvar:1 |