| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:143001472-143001631 | Common:2; Rare:57 | ||||
| chr3:143971711-143971829 | Common:1; Rare:54 | ||||
| chr3:143971938-143972081 | Common:1; Rare:52 | ||||
| chr3:146160840-146161386 | Common:3; Rare:172; Clinvar:5; Clinvar (benign):2 | ||||
| chr3:146250599-146251254 | Common:5; Rare:145 | ||||
| chr3:146544441-146544872 | Common:5; Rare:102 | ||||
| chr3:148991388-148991632 | Common:2; Rare:112; Clinvar (benign):1 | ||||
| chr3:149129549-149129711 | Common:1; Rare:68; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:149377511-149377822 | Common:1; Rare:83 | ||||
| chr3:149812462-149812768 | Common:1; Rare:78 | ||||
| chr3:149813087-149813292 | Common:1; Rare:73 | ||||
| chr3:149971160-149971330 | Common:3; Rare:75 | ||||
| chr3:150408170-150408352 | Common:2; Rare:78 | ||||
| chr3:150545771-150546072 | Common:4; Rare:85 | ||||
| chr3:150603139-150603528 | Common:3; Rare:147 |