| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:11586891-11586999 | Rare:36 | ||||
| chr16:11587152-11587313 | Common:1; Rare:39 | ||||
| chr16:11742830-11743090 | Common:2; Rare:106 | ||||
| chr16:11797176-11797499 | Common:2; Rare:124 | ||||
| chr16:11851406-11851635 | Common:1; Rare:118 | ||||
| chr16:11915841-11916219 | Common:2; Rare:153 | ||||
| chr16:11976609-11976766 | Common:3; Rare:61 | ||||
| chr16:13920078-13920213 | Common:2; Rare:68; Clinvar:4; Clinvar (benign):1 | ||||
| chr16:14071260-14071355 | Rare:35 | ||||
| chr16:14501659-14501774 | Rare:21 | ||||
| chr16:14630111-14630440 | Rare:140 | ||||
| chr16:14632695-14632983 | Common:1; Rare:101 | ||||
| chr16:14974682-14975191 | Common:2; Rare:137 | ||||
| chr16:15094212-15094415 | Common:1; Rare:102 | ||||
| chr16:15502150-15502210 | Rare:11 |