| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:86467410-86467620 | Common:2; Rare:59 | ||||
| chr16:86475910-86475994 | Rare:27 | ||||
| chr16:86477819-86478000 | Common:3; Rare:40 | ||||
| chr16:86488175-86488421 | Common:4; Rare:67 | ||||
| chr16:86488571-86488887 | Common:6; Rare:80 | ||||
| chr16:86489865-86490162 | Common:4; Rare:78 | ||||
| chr16:86503343-86503678 | Common:11; Rare:90 | ||||
| chr16:86503915-86504038 | Common:1; Rare:30 | ||||
| chr16:86507609-86508356 | Common:6; Rare:196 | ||||
| chr16:86508676-86509254 | Common:5; Rare:151 | ||||
| chr16:86509634-86509682 | Rare:11 | ||||
| chr16:86511071-86511805 | Common:2; Rare:266; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr16:86567835-86567935 | Rare:50 | ||||
| chr16:86568847-86568985 | Common:1; Rare:55 | ||||
| chr16:86569112-86569233 | Rare:28 |