| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:53055341-53055756 | Common:9; Rare:175 | ||||
| chr16:53098790-53099350 | Common:1; Rare:136 | ||||
| chr16:53099405-53099805 | Rare:153 | ||||
| chr16:53130330-53130687 | Common:10; Rare:208 | ||||
| chr16:53130749-53131061 | Common:3; Rare:243 | ||||
| chr16:53131027-53131914 | Common:17; Rare:450 | ||||
| chr16:53207700-53208060 | Common:4; Rare:139 | ||||
| chr16:53208080-53208700 | Rare:236 | ||||
| chr16:53209499-53209981 | Rare:193 | ||||
| chr16:53434229-53434629 | Common:5; Rare:314 | ||||
| chr16:53434882-53435282 | Common:3; Rare:157 | ||||
| chr16:53435379-53435780 | Common:4; Rare:163 | ||||
| chr16:53502441-53503776 | Common:50; Rare:1039 | ||||
| chr16:53703810-53704232 | Common:3; Rare:810; Clinvar:26; Clinvar (benign):9 | ||||
| chr16:54930450-54930870 | Common:5; Rare:283 |