| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:51030016-51030321 | Rare:104; Clinvar:3 | ||||
| chr18:51030578-51030799 | Common:1; Rare:82; Clinvar:2; Clinvar (benign):4 | ||||
| chr18:51196270-51196608 | Rare:102 | ||||
| chr18:51197359-51198155 | Rare:245 | ||||
| chr18:54269409-54269709 | Common:5; Rare:124 | ||||
| chr18:54269762-54269932 | Rare:49 | ||||
| chr18:54269972-54270247 | Common:2; Rare:68 | ||||
| chr18:54284991-54285164 | Common:1; Rare:42 | ||||
| chr18:54357732-54358021 | Common:9; Rare:88 | ||||
| chr18:54358585-54358645 | Rare:19 | ||||
| chr18:55321572-55321660 | Rare:22 | ||||
| chr18:55321739-55321959 | Rare:51 | ||||
| chr18:55322331-55322678 | Common:1; Rare:73 | ||||
| chr18:55322718-55322853 | Common:2; Rare:22 | ||||
| chr18:55589839-55590041 | Common:2; Rare:72 |