| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:30697937-30698235 | Common:1; Rare:133 | ||||
| chr16:30698457-30698644 | Common:1; Rare:72 | ||||
| chr16:30699046-30699199 | Rare:52; Clinvar (benign):1 | ||||
| chr16:30762047-30762360 | Common:3; Rare:101 | ||||
| chr16:30787157-30787495 | Common:1; Rare:72 | ||||
| chr16:30893868-30894275 | Common:5; Rare:108 | ||||
| chr16:30896425-30896635 | Common:2; Rare:49 | ||||
| chr16:30923124-30923151 | Rare:5 | ||||
| chr16:30923236-30923592 | Common:1; Rare:87 | ||||
| chr16:30948901-30949143 | Rare:39 | ||||
| chr16:31032826-31033096 | Common:1; Rare:53 | ||||
| chr16:31033456-31033760 | Common:1; Rare:87 | ||||
| chr16:31073726-31073848 | Rare:37 | ||||
| chr16:31074187-31074480 | Common:1; Rare:83 | ||||
| chr16:31094699-31094885 | Rare:59 |