| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:5097728-5098004 | Common:4; Rare:101 | ||||
| chr16:8674419-8674695 | Common:1; Rare:92; Clinvar:2 | ||||
| chr16:8797610-8797885 | Common:1; Rare:111; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:8861732-8862027 | Common:4; Rare:85 | ||||
| chr16:8868977-8869285 | Common:4; Rare:138 | ||||
| chr16:10385833-10386215 | Common:1; Rare:130 | ||||
| chr16:10580569-10580793 | Rare:74 | ||||
| chr16:10743790-10743882 | Rare:37 | ||||
| chr16:10944316-10944634 | Common:1; Rare:100 | ||||
| chr16:11851493-11851635 | Rare:73 | ||||
| chr16:11915370-11915487 | Common:4; Rare:52 | ||||
| chr16:11915889-11916215 | Common:2; Rare:134 | ||||
| chr16:11976609-11976766 | Common:3; Rare:61 | ||||
| chr16:14630137-14630404 | Rare:119 | ||||
| chr16:14632747-14632990 | Common:1; Rare:78 |