| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:87317384-87317511 | Common:3; Rare:48 | ||||
| chr16:87383755-87383960 | Common:1; Rare:88 | ||||
| chr16:87765901-87766028 | Rare:52 | ||||
| chr16:88570179-88570498 | Common:1; Rare:122 | ||||
| chr16:88663079-88663374 | Common:8; Rare:121 | ||||
| chr16:88706210-88706542 | Common:4; Rare:147 | ||||
| chr16:88715976-88716269 | Common:2; Rare:142; Clinvar (benign):1 | ||||
| chr16:88717056-88717355 | Common:3; Rare:131; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr16:88719672-88719912 | Common:3; Rare:103 | ||||
| chr16:88725414-88725635 | Common:1; Rare:105 | ||||
| chr16:88732494-88732703 | Common:1; Rare:108; Clinvar:1; Clinvar (benign):1 | ||||
| chr16:88810143-88810559 | Common:8; Rare:158; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr16:88811554-88811840 | Common:4; Rare:103; Clinvar:1; Clinvar (benign):2 | ||||
| chr16:88811880-88812093 | Common:2; Rare:87; Clinvar (benign):1 | ||||
| chr16:88856932-88857174 | Common:4; Rare:109; Clinvar (benign):2 |