| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:54828370-54828860 | Common:5; Rare:108 | ||||
| chr18:55401978-55402118 | Common:1; Rare:24 | ||||
| chr18:55585694-55586407 | Common:7; Rare:259 | ||||
| chr18:55587181-55587468 | Rare:34 | ||||
| chr18:55587501-55587660 | Common:1; Rare:34 | ||||
| chr18:55588182-55588355 | Rare:39; Clinvar:2 | ||||
| chr18:55589842-55590041 | Common:2; Rare:70 | ||||
| chr18:56638553-56638914 | Common:5; Rare:130 | ||||
| chr18:56651068-56651416 | Common:5; Rare:93 | ||||
| chr18:56756922-56757322 | Rare:172 | ||||
| chr18:57435212-57435411 | Rare:47 | ||||
| chr18:57586600-57586970 | Common:1; Rare:87; Clinvar (benign):1 | ||||
| chr18:57621692-57621972 | Common:3; Rare:95 | ||||
| chr18:58043960-58044360 | Common:4; Rare:169 | ||||
| chr18:58044541-58045302 | Common:8; Rare:265 |