| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:14071269-14071382 | Common:1; Rare:47 | ||||
| chr16:14186552-14186725 | Rare:35 | ||||
| chr16:14630145-14630405 | Rare:118 | ||||
| chr16:14632747-14632987 | Common:1; Rare:77 | ||||
| chr16:14974268-14974591 | Rare:34 | ||||
| chr16:14974693-14975480 | Common:3; Rare:175 | ||||
| chr16:14976457-14976738 | Common:1; Rare:15 | ||||
| chr16:15055957-15056282 | Common:2; Rare:107 | ||||
| chr16:15094229-15094454 | Common:1; Rare:113 | ||||
| chr16:15395900-15396150 | Rare:94 | ||||
| chr16:15643005-15643272 | Rare:82 | ||||
| chr16:15650078-15650293 | Common:1; Rare:110 | ||||
| chr16:15711253-15711391 | Rare:42 | ||||
| chr16:15741765-15742069 | Common:1; Rare:80; Clinvar:2; Clinvar (benign):2 | ||||
| chr16:15742254-15742398 | Common:1; Rare:20 |