| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:77722314-77722585 | Common:3; Rare:97 | ||||
| chr16:79600721-79600887 | Common:1; Rare:49 | ||||
| chr16:81006413-81006553 | Rare:36 | ||||
| chr16:81006798-81007211 | Common:5; Rare:140 | ||||
| chr16:84116770-84117066 | Common:4; Rare:119 | ||||
| chr16:84145121-84145257 | Rare:77 | ||||
| chr16:84187025-84187306 | Common:3; Rare:93 | ||||
| chr16:84504616-84504823 | Common:5; Rare:87 | ||||
| chr16:85027627-85027822 | Common:1; Rare:101 | ||||
| chr16:85799064-85799067 | |||||
| chr16:85799520-85799771 | Common:2; Rare:76 | ||||
| chr16:86555180-86555304 | Rare:62 | ||||
| chr16:87765924-87766017 | Rare:38 | ||||
| chr16:88570174-88570416 | Common:1; Rare:87 | ||||
| chr16:88650986-88651140 | Common:1; Rare:50; Clinvar (benign):1; Clinvar (pathogenic):1 |