| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:1615067-1615315 | Common:1; Rare:67 | ||||
| chr16:1677993-1678636 | Common:6; Rare:200 | ||||
| chr16:1678662-1678793 | Common:3; Rare:36 | ||||
| chr16:1705733-1705872 | Common:1; Rare:31 | ||||
| chr16:1705900-1706374 | Common:4; Rare:149 | ||||
| chr16:1706592-1706638 | Rare:6 | ||||
| chr16:1770514-1771023 | Common:3; Rare:254 | ||||
| chr16:1771468-1771626 | Rare:69 | ||||
| chr16:1772389-1772550 | Common:1; Rare:71 | ||||
| chr16:1772677-1772920 | Common:2; Rare:75; Clinvar (pathogenic):1 | ||||
| chr16:1773054-1773278 | Rare:91; Clinvar (pathogenic):1 | ||||
| chr16:1773409-1773714 | Common:1; Rare:139 | ||||
| chr16:1780905-1781277 | Rare:112 | ||||
| chr16:1781826-1781965 | Common:1; Rare:32 | ||||
| chr16:1782404-1783058 | Common:4; Rare:228 |