| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:50281436-50281914 | Common:3; Rare:159 | ||||
| chr18:50374875-50375176 | Common:4; Rare:95 | ||||
| chr18:50559948-50560193 | Common:4; Rare:76 | ||||
| chr18:50878943-50879254 | Common:4; Rare:102 | ||||
| chr18:50967875-50968087 | Rare:77 | ||||
| chr18:51030029-51030222 | Rare:68 | ||||
| chr18:54269449-54269630 | Common:2; Rare:87 | ||||
| chr18:54357631-54357666 | Rare:6 | ||||
| chr18:54357838-54357977 | Common:6; Rare:44 | ||||
| chr18:54828303-54828587 | Rare:69 | ||||
| chr18:54828597-54828800 | Common:4; Rare:43 | ||||
| chr18:55321758-55321929 | Rare:38 | ||||
| chr18:55322167-55322647 | Common:1; Rare:90 | ||||
| chr18:55588095-55588323 | Rare:54; Clinvar:3; Clinvar (benign):1 | ||||
| chr18:55589713-55590016 | Common:2; Rare:101 |