| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:86568798-86568859 | Rare:35; Clinvar (benign):1 | ||||
| chr16:86568949-86569378 | Common:2; Rare:97 | ||||
| chr16:86569388-86569506 | Rare:19 | ||||
| chr16:86569528-86569725 | Common:4; Rare:42 | ||||
| chr16:86570151-86570297 | Common:2; Rare:39 | ||||
| chr16:86664539-86664761 | Common:2; Rare:54 | ||||
| chr16:86824404-86824586 | Common:2; Rare:47 | ||||
| chr16:86827484-86827850 | Common:3; Rare:69 | ||||
| chr16:86836728-86836994 | Common:5; Rare:42 | ||||
| chr16:86929173-86929468 | Common:6; Rare:81 | ||||
| chr16:86929759-86929807 | Common:2; Rare:12 | ||||
| chr16:86930207-86930402 | Common:2; Rare:54 | ||||
| chr16:86931215-86931696 | Common:4; Rare:117 | ||||
| chr16:86951808-86952112 | Common:4; Rare:81 | ||||
| chr16:87053095-87053211 | Common:1; Rare:36 |