| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:51030048-51030238 | Rare:63 | ||||
| chr18:54224575-54224808 | Common:1; Rare:62 | ||||
| chr18:54269803-54269830 | Rare:7 | ||||
| chr18:54357860-54357924 | Common:1; Rare:18 | ||||
| chr18:54828558-54828639 | Rare:12 | ||||
| chr18:55321786-55321920 | Rare:28 | ||||
| chr18:55401678-55401990 | Rare:57 | ||||
| chr18:55589707-55589894 | Rare:52 | ||||
| chr18:56651125-56651552 | Common:5; Rare:105 | ||||
| chr18:56651600-56651708 | Common:4; Rare:27 | ||||
| chr18:57621713-57621959 | Common:3; Rare:88 | ||||
| chr18:57803050-57803452 | Common:4; Rare:107; Clinvar (benign):1 | ||||
| chr18:58045545-58045745 | Rare:56 | ||||
| chr18:59697332-59697744 | Common:2; Rare:132; Clinvar:1 | ||||
| chr18:59899809-59899997 | Common:3; Rare:59 |