| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:12702627-12703097 | Common:3; Rare:183 | ||||
| chr18:12947694-12948061 | Common:3; Rare:89 | ||||
| chr18:12991143-12991410 | Common:2; Rare:98 | ||||
| chr18:13726431-13726724 | Common:4; Rare:112 | ||||
| chr18:21111038-21111097 | Rare:16 | ||||
| chr18:21111102-21111370 | Common:1; Rare:62 | ||||
| chr18:21111522-21111985 | Common:2; Rare:143 | ||||
| chr18:21242192-21242343 | Common:1; Rare:62 | ||||
| chr18:21600480-21600778 | Rare:82 | ||||
| chr18:21600831-21600913 | Rare:24 | ||||
| chr18:22933267-22933426 | Common:2; Rare:66; Clinvar:3; Clinvar (benign):2 | ||||
| chr18:22933807-22933867 | Common:1; Rare:23 | ||||
| chr18:23453156-23453359 | Rare:73 | ||||
| chr18:23503293-23503621 | Common:4; Rare:139 | ||||
| chr18:23586350-23586563 | Common:4; Rare:92; Clinvar:6; Clinvar (benign):3 |