| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:31072642-31072775 | Rare:25 | ||||
| chr16:31073014-31073137 | Common:1; Rare:28 | ||||
| chr16:31073156-31073344 | Rare:49 | ||||
| chr16:31073356-31073427 | Common:1; Rare:19 | ||||
| chr16:31073428-31073516 | Rare:29 | ||||
| chr16:31073636-31073883 | Rare:70 | ||||
| chr16:31074134-31074483 | Common:3; Rare:99 | ||||
| chr16:31093203-31093378 | Rare:52; Clinvar:1 | ||||
| chr16:31094568-31094831 | Common:1; Rare:98; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr16:31094841-31094933 | Rare:19; Clinvar:1 | ||||
| chr16:31094938-31095040 | Rare:22 | ||||
| chr16:31108274-31108507 | Rare:50 | ||||
| chr16:31117452-31117748 | Common:2; Rare:88 | ||||
| chr16:31117816-31118182 | Rare:83 | ||||
| chr16:31135653-31135762 | Rare:28 |