| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:57819761-57819983 | Rare:50 | ||||
| chr18:58115268-58115406 | Rare:26 | ||||
| chr18:58315772-58315938 | Rare:47 | ||||
| chr18:58914131-58914316 | Common:1; Rare:19 | ||||
| chr18:58937270-58937517 | Common:3; Rare:37 | ||||
| chr18:58980719-58980848 | Rare:31 | ||||
| chr18:58992889-58992915 | Rare:5 | ||||
| chr18:58992932-58992993 | Common:1; Rare:17 | ||||
| chr18:59352314-59352348 | Rare:5 | ||||
| chr18:59355313-59355656 | Common:1; Rare:95; Clinvar (benign):2 | ||||
| chr18:59873670-59873892 | Rare:32 | ||||
| chr18:60455230-60455360 | Common:3; Rare:32 | ||||
| chr18:61606870-61607102 | Rare:52 | ||||
| chr18:61874781-61874797 | Rare:2 | ||||
| chr18:62068605-62068630 | Rare:2 |