Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:146160963-146161388 | Common:2; Rare:128; Clinvar:5; Clinvar (benign):2 | ||||
chr3:148857426-148857605 | Common:1; Rare:54 | ||||
chr3:149377632-149377844 | Common:1; Rare:50 | ||||
chr3:149813107-149813300 | Common:1; Rare:72 | ||||
chr3:150408093-150408308 | Common:1; Rare:73 | ||||
chr3:150603151-150603342 | Common:2; Rare:71 | ||||
chr3:152268691-152269142 | Rare:163 | ||||
chr3:152269160-152269337 | Rare:46 | ||||
chr3:152269544-152269677 | Rare:36 | ||||
chr3:154121264-154121451 | Common:2; Rare:80 | ||||
chr3:154324303-154324521 | Rare:95 | ||||
chr3:155853522-155853711 | Common:1; Rare:46; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr3:155854364-155854804 | Rare:127 | ||||
chr3:155870323-155870761 | Common:2; Rare:122 | ||||
chr3:156674355-156674647 | Common:3; Rare:87 |