| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:142723907-142724045 | Rare:40 | ||||
| chr3:143001454-143001661 | Common:2; Rare:78 | ||||
| chr3:143971607-143971825 | Common:1; Rare:94 | ||||
| chr3:143971863-143972074 | Rare:73 | ||||
| chr3:143973798-143974079 | Common:1; Rare:60 | ||||
| chr3:146160962-146161386 | Common:2; Rare:128; Clinvar:5; Clinvar (benign):2 | ||||
| chr3:146250971-146251364 | Common:2; Rare:97 | ||||
| chr3:146544458-146544962 | Common:5; Rare:124 | ||||
| chr3:149129542-149129693 | Common:1; Rare:59; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:149377600-149377818 | Common:1; Rare:52 | ||||
| chr3:149657964-149658245 | Rare:64 | ||||
| chr3:149812984-149813297 | Common:2; Rare:104 | ||||
| chr3:149971153-149971342 | Common:3; Rare:86 | ||||
| chr3:150408079-150408320 | Common:2; Rare:81 | ||||
| chr3:150603147-150603404 | Common:2; Rare:103 |