Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:16264864-16265229 | Common:2; Rare:122 | ||||
chr3:16512902-16512954 | Rare:8 | ||||
chr3:17742596-17742938 | Common:4; Rare:116 | ||||
chr3:19946972-19947450 | Common:7; Rare:177 | ||||
chr3:20186139-20186355 | Common:3; Rare:65 | ||||
chr3:21751086-21751415 | Common:4; Rare:106 | ||||
chr3:23916863-23917231 | Rare:139 | ||||
chr3:23917589-23918031 | Common:2; Rare:116; Clinvar (benign):1 | ||||
chr3:25428103-25428398 | Rare:67 | ||||
chr3:25783392-25783647 | Common:2; Rare:80; Clinvar (benign):3 | ||||
chr3:25790006-25790118 | Common:3; Rare:43 | ||||
chr3:28348616-28348721 | Rare:24 | ||||
chr3:28348779-28349178 | Common:3; Rare:127 | ||||
chr3:29280868-29281388 | Common:15; Rare:100 | ||||
chr3:30606394-30606546 | Common:1; Rare:36; Clinvar:2 |