| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:5071952-5072352 | Common:5; Rare:173; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr16:5097735-5098089 | Common:8; Rare:191 | ||||
| chr16:8621608-8621757 | Common:2; Rare:111 | ||||
| chr16:8674409-8674699 | Common:2; Rare:189; Clinvar:4 | ||||
| chr16:8797552-8797939 | Common:4; Rare:282; Clinvar:6; Clinvar (benign):4; Clinvar (pathogenic):6 | ||||
| chr16:8868160-8868560 | Common:2; Rare:129 | ||||
| chr16:8868956-8869312 | Common:10; Rare:288 | ||||
| chr16:8963829-8964115 | Common:3; Rare:164 | ||||
| chr16:9091140-9091723 | Common:3; Rare:309 | ||||
| chr16:9091670-9092172 | Common:1; Rare:326 | ||||
| chr16:10385854-10386238 | Common:1; Rare:208 | ||||
| chr16:10580586-10580853 | Common:2; Rare:91 | ||||
| chr16:10743740-10743880 | Rare:99 | ||||
| chr16:10744020-10744320 | Common:3; Rare:218 | ||||
| chr16:10944369-10944594 | Common:1; Rare:66 |