| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:3148735-3148985 | Rare:66 | ||||
| chr16:4307585-4307834 | Common:3; Rare:86 | ||||
| chr16:4866855-4867001 | Common:3; Rare:34 | ||||
| chr16:4887160-4887389 | Common:2; Rare:74 | ||||
| chr16:8644977-8645265 | Common:2; Rare:80 | ||||
| chr16:8847485-8847951 | Common:2; Rare:197; Clinvar:12; Clinvar (benign):7; Clinvar (pathogenic):8 | ||||
| chr16:14824735-14825049 | Rare:45 | ||||
| chr16:14876427-14876746 | Rare:77 | ||||
| chr16:15017183-15017364 | Common:1; Rare:39 | ||||
| chr16:15022425-15022711 | Common:1; Rare:41 | ||||
| chr16:15028655-15028938 | Rare:61 | ||||
| chr16:15029755-15030055 | Common:2; Rare:55 | ||||
| chr16:15035286-15035515 | Common:2; Rare:79 | ||||
| chr16:15035944-15035973 | Rare:9 | ||||
| chr16:15715163-15715398 | Common:1; Rare:64; Clinvar:4; Clinvar (benign):8 |