| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:970832-971135 | Common:7; Rare:144 | ||||
| chr16:1309381-1309755 | Rare:139 | ||||
| chr16:1351911-1352002 | Rare:56; Clinvar:5 | ||||
| chr16:1420718-1420939 | Common:1; Rare:89 | ||||
| chr16:1493253-1493587 | Common:4; Rare:101 | ||||
| chr16:1533492-1533694 | Common:1; Rare:39 | ||||
| chr16:1612037-1612360 | Common:2; Rare:108; Clinvar:1 | ||||
| chr16:1706086-1706245 | Common:1; Rare:47 | ||||
| chr16:1771499-1771847 | Common:3; Rare:138 | ||||
| chr16:1772858-1773187 | Common:3; Rare:116; Clinvar (pathogenic):2 | ||||
| chr16:1782508-1782850 | Common:4; Rare:115 | ||||
| chr16:1826770-1826949 | Common:3; Rare:55 | ||||
| chr16:1827161-1827238 | Common:1; Rare:36 | ||||
| chr16:1943154-1943508 | Common:1; Rare:111 | ||||
| chr16:1964802-1965061 | Common:6; Rare:122 |