| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:57628504-57628706 | Common:3; Rare:50 | ||||
| chr16:57735209-57735874 | Common:8; Rare:163 | ||||
| chr16:57735965-57736042 | Rare:14 | ||||
| chr16:57736235-57736468 | Rare:32 | ||||
| chr16:57736548-57736777 | Common:1; Rare:38 | ||||
| chr16:57764333-57764528 | Rare:40 | ||||
| chr16:57801870-57802194 | Common:1; Rare:60 | ||||
| chr16:57802355-57802668 | Common:1; Rare:63 | ||||
| chr16:57802714-57802764 | Rare:11 | ||||
| chr16:57802944-57803009 | Rare:18 | ||||
| chr16:57938987-57939193 | Common:1; Rare:54 | ||||
| chr16:57939349-57939506 | Rare:48 | ||||
| chr16:57976306-57976502 | Rare:34 | ||||
| chr16:58000535-58000909 | Common:2; Rare:92 | ||||
| chr16:58001176-58001635 | Common:2; Rare:131; Clinvar (benign):1 |