| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:14071024-14071370 | Common:4; Rare:117 | ||||
| chr16:14186475-14186725 | Rare:45 | ||||
| chr16:14630206-14630462 | Rare:101 | ||||
| chr16:14632723-14632990 | Common:1; Rare:89 | ||||
| chr16:15741776-15742007 | Common:1; Rare:68; Clinvar:2; Clinvar (benign):2 | ||||
| chr16:15856954-15857151 | Common:2; Rare:41; Clinvar:1; Clinvar (benign):2 | ||||
| chr16:20806337-20806520 | Rare:66 | ||||
| chr16:20900515-20900873 | Common:2; Rare:88 | ||||
| chr16:21953038-21953413 | Common:1; Rare:96; Clinvar (benign):3 | ||||
| chr16:23453137-23453183 | Rare:18 | ||||
| chr16:23641278-23641517 | Common:2; Rare:65; Clinvar:1; Clinvar (benign):2 | ||||
| chr16:25111453-25111762 | Common:2; Rare:72 | ||||
| chr16:27268719-27268891 | Common:1; Rare:62 | ||||
| chr16:27549886-27550167 | Common:2; Rare:104 | ||||
| chr16:28822573-28822752 | Rare:68 |