| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:42054767-42054885 | Rare:18 | ||||
| chr18:42080981-42081241 | Rare:68 | ||||
| chr18:42933823-42934018 | Rare:45 | ||||
| chr18:44749754-44749971 | Rare:32 | ||||
| chr18:46084316-46084532 | Rare:49; Clinvar (benign):2 | ||||
| chr18:47076304-47076356 | Rare:11 | ||||
| chr18:47103610-47103671 | Rare:15 | ||||
| chr18:47912739-47912855 | Common:1; Rare:15 | ||||
| chr18:48569109-48569198 | Rare:13 | ||||
| chr18:48646932-48647152 | Common:4; Rare:42 | ||||
| chr18:49009602-49009912 | Common:1; Rare:49 | ||||
| chr18:49021509-49021725 | Common:1; Rare:41 | ||||
| chr18:49174600-49174835 | Rare:36 | ||||
| chr18:49488983-49489162 | Rare:36 | ||||
| chr18:49564736-49564885 | Rare:25 |