| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:75464352-75464448 | Common:4; Rare:43 | ||||
| chr16:75555266-75555417 | Common:1; Rare:35 | ||||
| chr16:75556214-75556427 | Common:1; Rare:76; Clinvar (benign):3 | ||||
| chr16:75623216-75623421 | Common:3; Rare:78 | ||||
| chr16:75647584-75647848 | Common:3; Rare:131; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr16:75648636-75648749 | Rare:45 | ||||
| chr16:77190681-77191015 | Common:12; Rare:109 | ||||
| chr16:77191086-77191239 | Common:2; Rare:63 | ||||
| chr16:77722319-77722556 | Common:3; Rare:80 | ||||
| chr16:78099296-78099731 | Common:2; Rare:171 | ||||
| chr16:81006430-81006567 | Rare:42 | ||||
| chr16:81006786-81007277 | Common:5; Rare:168 | ||||
| chr16:81077186-81077328 | Common:1; Rare:68 | ||||
| chr16:81314775-81315023 | Common:2; Rare:118; Clinvar:2 | ||||
| chr16:82170123-82170358 | Common:7; Rare:127 |