| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:141875989-141876262 | Rare:73 | ||||
| chr3:141876446-141876665 | Common:1; Rare:82 | ||||
| chr3:142225538-142225675 | Common:1; Rare:43 | ||||
| chr3:143001454-143001626 | Common:2; Rare:61 | ||||
| chr3:143971713-143971830 | Common:1; Rare:51 | ||||
| chr3:146160961-146161386 | Common:2; Rare:129; Clinvar:5; Clinvar (benign):2 | ||||
| chr3:146250596-146250674 | Rare:14 | ||||
| chr3:146544467-146544865 | Common:5; Rare:95 | ||||
| chr3:148991388-148991632 | Common:2; Rare:112; Clinvar (benign):1 | ||||
| chr3:149129545-149129676 | Common:1; Rare:48; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:149377621-149378002 | Common:1; Rare:74 | ||||
| chr3:149812919-149813291 | Common:2; Rare:110 | ||||
| chr3:149970864-149971082 | Common:1; Rare:100 | ||||
| chr3:150408002-150408302 | Common:1; Rare:88 | ||||
| chr3:150603157-150603387 | Common:2; Rare:90 |