| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:141876770-141876910 | Rare:53 | ||||
| chr3:142028540-142029030 | Common:7; Rare:89 | ||||
| chr3:142029050-142029935 | Common:8; Rare:215 | ||||
| chr3:142148667-142149521 | Common:9; Rare:306 | ||||
| chr3:142149458-142149648 | Common:1; Rare:48 | ||||
| chr3:142225360-142225910 | Common:19; Rare:592 | ||||
| chr3:142447288-142448281 | Common:14; Rare:752 | ||||
| chr3:142578033-142578691 | Common:1; Rare:141; Clinvar (benign):1 | ||||
| chr3:142578680-142579148 | Common:1; Rare:1030; Clinvar:9; Clinvar (benign):5 | ||||
| chr3:142596022-142596690 | Common:14; Rare:401 | ||||
| chr3:142723781-142724181 | Common:5; Rare:318 | ||||
| chr3:142724190-142724600 | Common:12; Rare:257 | ||||
| chr3:142724620-142724880 | Common:1; Rare:73 | ||||
| chr3:142724900-142725360 | Common:1; Rare:151 | ||||
| chr3:142888563-142889580 | Common:10; Rare:314 |