| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:75464598-75464780 | Common:1; Rare:69 | ||||
| chr16:75495368-75495592 | Common:2; Rare:85 | ||||
| chr16:75555241-75555545 | Common:5; Rare:63 | ||||
| chr16:75556207-75556421 | Common:2; Rare:79; Clinvar (benign):4 | ||||
| chr16:75566202-75566434 | Common:2; Rare:110 | ||||
| chr16:75622822-75622891 | Rare:23 | ||||
| chr16:75623200-75623585 | Common:4; Rare:130 | ||||
| chr16:75647443-75647969 | Common:5; Rare:231; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr16:75648040-75648234 | Rare:84 | ||||
| chr16:75648608-75648744 | Rare:55 | ||||
| chr16:77190593-77190730 | Common:4; Rare:46 | ||||
| chr16:77190842-77191088 | Common:5; Rare:79 | ||||
| chr16:77191113-77191252 | Common:1; Rare:59 | ||||
| chr16:77191523-77191582 | Common:2; Rare:28 | ||||
| chr16:77191696-77191804 | Rare:25 |