| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:75433395-75433812 | Common:4; Rare:124 | ||||
| chr16:75433844-75433959 | Common:1; Rare:37 | ||||
| chr16:75464352-75464448 | Common:4; Rare:43 | ||||
| chr16:75566241-75566446 | Common:1; Rare:106 | ||||
| chr16:75647614-75647829 | Common:2; Rare:107; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr16:77190683-77191015 | Common:11; Rare:109 | ||||
| chr16:77191122-77191246 | Common:1; Rare:54 | ||||
| chr16:79600721-79600958 | Common:1; Rare:66 | ||||
| chr16:80540925-80541025 | Common:2; Rare:36 | ||||
| chr16:81006430-81006538 | Rare:30 | ||||
| chr16:81006791-81007255 | Common:5; Rare:155 | ||||
| chr16:81077231-81077319 | Common:1; Rare:41 | ||||
| chr16:81314768-81315071 | Common:3; Rare:145; Clinvar:4; Clinvar (benign):1 | ||||
| chr16:82035013-82035431 | Common:1; Rare:102 | ||||
| chr16:82170132-82170291 | Common:6; Rare:87 |