| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:75566192-75566434 | Common:2; Rare:111 | ||||
| chr16:75621921-75622005 | Common:1; Rare:24 | ||||
| chr16:75623215-75623440 | Common:3; Rare:85 | ||||
| chr16:75647269-75647339 | Common:1; Rare:14 | ||||
| chr16:75647438-75648008 | Common:5; Rare:241; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr16:75648039-75648246 | Rare:86 | ||||
| chr16:75648426-75648766 | Rare:131 | ||||
| chr16:77190609-77191292 | Common:16; Rare:241 | ||||
| chr16:77722272-77722653 | Common:4; Rare:137 | ||||
| chr16:78099249-78099459 | Common:2; Rare:80 | ||||
| chr16:78099501-78099779 | Common:2; Rare:123; Clinvar (benign):5 | ||||
| chr16:78100058-78100152 | Rare:30 | ||||
| chr16:80540768-80541040 | Common:5; Rare:119 | ||||
| chr16:80803773-80803794 | Rare:3 | ||||
| chr16:80804528-80804672 | Rare:43 |