| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:89701631-89701841 | Common:1; Rare:79 | ||||
| chr16:89720660-89721066 | Common:3; Rare:179 | ||||
| chr16:89721221-89721616 | Common:6; Rare:245 | ||||
| chr16:89722640-89723090 | Common:2; Rare:189 | ||||
| chr16:89808402-89809050 | Common:10; Rare:243 | ||||
| chr16:89816502-89816954 | Common:15; Rare:390; Clinvar:14; Clinvar (benign):8; Clinvar (pathogenic):8 | ||||
| chr16:89817652-89817921 | Common:3; Rare:135 | ||||
| chr16:89828253-89828597 | Common:6; Rare:256 | ||||
| chr16:89828758-89828987 | Rare:68 | ||||
| chr16:89873428-89873807 | Common:9; Rare:284 | ||||
| chr16:89921620-89922020 | Common:1; Rare:162 | ||||
| chr16:89923117-89923348 | Rare:171 | ||||
| chr16:89948672-89948799 | Common:2; Rare:31 | ||||
| chr16:89972455-89972800 | Common:3; Rare:191 | ||||
| chr16:89972805-89972926 | Common:2; Rare:72 |