| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:141368513-141368540 | Rare:4 | ||||
| chr3:141402235-141402443 | Common:2; Rare:59 | ||||
| chr3:141431974-141432185 | Common:2; Rare:32 | ||||
| chr3:141875989-141876246 | Rare:71 | ||||
| chr3:141876439-141876751 | Common:2; Rare:119 | ||||
| chr3:142225469-142225660 | Common:3; Rare:66 | ||||
| chr3:142447968-142448126 | Common:1; Rare:55 | ||||
| chr3:142578711-142578948 | Rare:83; Clinvar:1 | ||||
| chr3:142723909-142724068 | Rare:46 | ||||
| chr3:143001472-143001650 | Common:2; Rare:67 | ||||
| chr3:143971711-143971847 | Common:1; Rare:64 | ||||
| chr3:143971967-143972074 | Rare:42 | ||||
| chr3:146160910-146161386 | Common:2; Rare:150; Clinvar:5; Clinvar (benign):2 | ||||
| chr3:146250969-146251217 | Common:1; Rare:57 | ||||
| chr3:146544458-146544970 | Common:5; Rare:124 |