| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:141402235-141402428 | Common:2; Rare:57 | ||||
| chr3:141486874-141487074 | Common:1; Rare:62 | ||||
| chr3:141876049-141876246 | Rare:55 | ||||
| chr3:141876452-141876665 | Common:1; Rare:78 | ||||
| chr3:142225491-142225660 | Common:3; Rare:58 | ||||
| chr3:142447968-142448110 | Common:1; Rare:50 | ||||
| chr3:142578711-142578948 | Rare:83; Clinvar:1 | ||||
| chr3:142723884-142724034 | Rare:41 | ||||
| chr3:143001453-143001632 | Common:2; Rare:64 | ||||
| chr3:143971631-143971831 | Common:1; Rare:88 | ||||
| chr3:143971967-143972074 | Rare:42 | ||||
| chr3:146160967-146161386 | Common:2; Rare:128; Clinvar:5; Clinvar (benign):2 | ||||
| chr3:146250984-146251229 | Common:1; Rare:61 | ||||
| chr3:146544623-146544952 | Common:1; Rare:86 | ||||
| chr3:147389037-147389088 | Rare:15 |