| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:13218673-13218790 | Common:1; Rare:25 | ||||
| chr18:13726473-13726729 | Common:3; Rare:98 | ||||
| chr18:21111017-21111439 | Common:1; Rare:100 | ||||
| chr18:21111518-21112031 | Common:3; Rare:160 | ||||
| chr18:21242192-21242387 | Common:1; Rare:82 | ||||
| chr18:21600649-21600804 | Rare:39 | ||||
| chr18:21600853-21600944 | Common:2; Rare:31 | ||||
| chr18:21704674-21704960 | Common:3; Rare:94 | ||||
| chr18:22169465-22169595 | Rare:36 | ||||
| chr18:22170558-22170892 | Common:1; Rare:64 | ||||
| chr18:22933260-22933446 | Common:2; Rare:73; Clinvar:4; Clinvar (benign):2 | ||||
| chr18:22933807-22933889 | Common:1; Rare:31 | ||||
| chr18:23453156-23453368 | Rare:76 | ||||
| chr18:23503220-23503601 | Common:4; Rare:152 | ||||
| chr18:23586360-23586530 | Common:4; Rare:70; Clinvar:6; Clinvar (benign):3 |