Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:143001405-143001631 | Common:3; Rare:85 | ||||
chr3:146160939-146161386 | Common:2; Rare:138; Clinvar:5; Clinvar (benign):2 | ||||
chr3:146544514-146544847 | Common:4; Rare:78 | ||||
chr3:148991383-148991632 | Common:2; Rare:115; Clinvar (benign):1 | ||||
chr3:149086471-149086711 | Rare:71 | ||||
chr3:149129549-149129714 | Common:1; Rare:69; Clinvar:2; Clinvar (benign):1 | ||||
chr3:149377609-149377834 | Common:1; Rare:54 | ||||
chr3:149657989-149658181 | Rare:41 | ||||
chr3:149812947-149813291 | Common:2; Rare:108 | ||||
chr3:150408169-150408302 | Common:1; Rare:54 | ||||
chr3:150603151-150603364 | Common:2; Rare:85 | ||||
chr3:150703900-150704013 | Rare:40 | ||||
chr3:152268817-152268977 | Rare:63 | ||||
chr3:152269549-152269678 | Rare:34 | ||||
chr3:153162036-153162238 | Rare:64 |