| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:4767126-4767330 | Common:1; Rare:67 | ||||
| chr16:5033933-5033987 | Rare:20 | ||||
| chr16:5065904-5066076 | Rare:73 | ||||
| chr16:5097746-5098025 | Common:4; Rare:93 | ||||
| chr16:7422660-7422787 | Common:2; Rare:39 | ||||
| chr16:8674412-8674686 | Common:1; Rare:93; Clinvar:2 | ||||
| chr16:8797624-8797866 | Rare:92; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:8868970-8869251 | Common:4; Rare:125 | ||||
| chr16:10580575-10580756 | Rare:57 | ||||
| chr16:10743528-10743855 | Common:1; Rare:100 | ||||
| chr16:10944326-10944634 | Common:1; Rare:95 | ||||
| chr16:11668248-11668508 | Common:3; Rare:115 | ||||
| chr16:11851517-11851645 | Rare:61 | ||||
| chr16:11915898-11916229 | Common:2; Rare:131 | ||||
| chr16:11976611-11976766 | Common:3; Rare:59 |