| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:53054760-53055059 | Common:2; Rare:65 | ||||
| chr16:53208437-53208600 | Rare:26 | ||||
| chr16:53703809-53704221 | Common:1; Rare:132; Clinvar:4; Clinvar (benign):2 | ||||
| chr16:54286714-54287011 | Common:1; Rare:89 | ||||
| chr16:56425074-56425143 | Rare:14 | ||||
| chr16:56451086-56451763 | Common:5; Rare:221 | ||||
| chr16:56608520-56608742 | Common:2; Rare:69 | ||||
| chr16:56657979-56658012 | Common:1; Rare:8 | ||||
| chr16:56682285-56682527 | Common:4; Rare:86 | ||||
| chr16:56729949-56730198 | Common:1; Rare:60 | ||||
| chr16:56831711-56832004 | Rare:75; Clinvar (pathogenic):1 | ||||
| chr16:56931941-56932289 | Common:2; Rare:181 | ||||
| chr16:56989382-56989585 | Common:1; Rare:47; Clinvar:1 | ||||
| chr16:57145924-57146322 | Common:1; Rare:111 | ||||
| chr16:57185581-57185621 | Rare:6 |