Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:156674373-156674618 | Common:3; Rare:67 | ||||
chr3:158732182-158732268 | Common:2; Rare:28 | ||||
chr3:158732414-158732728 | Common:3; Rare:102 | ||||
chr3:160399177-160399307 | Rare:35; Clinvar:2 | ||||
chr3:160399514-160399675 | Rare:36 | ||||
chr3:160565385-160565845 | Common:2; Rare:164 | ||||
chr3:167734822-167735198 | Common:2; Rare:117; Clinvar:1; Clinvar (benign):1 | ||||
chr3:167735597-167735752 | Rare:40 | ||||
chr3:169773316-169773424 | Rare:36 | ||||
chr3:169966736-169966842 | Rare:46 | ||||
chr3:169982899-169983209 | Common:1; Rare:57 | ||||
chr3:170222317-170222539 | Common:2; Rare:72 | ||||
chr3:179604632-179604864 | Common:2; Rare:84 | ||||
chr3:180989626-180989790 | Rare:74; Clinvar:1; Clinvar (benign):1 | ||||
chr3:184155297-184155496 | Rare:62 |