Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:45857350-45857617 | Common:3; Rare:67 | ||||
chr20:45891178-45891400 | Common:1; Rare:70; Clinvar:3; Clinvar (benign):1 | ||||
chr20:50958521-50958823 | Common:1; Rare:89; Clinvar (benign):1 | ||||
chr20:58910056-58910370 | Rare:85 | ||||
chr20:63707881-63708027 | Rare:45 | ||||
chr21:25734870-25734967 | Common:2; Rare:42 | ||||
chr21:31659502-31659837 | Common:2; Rare:150; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):7 | ||||
chr21:33542829-33543090 | Common:2; Rare:95 | ||||
chr21:37073069-37073235 | Common:4; Rare:62 | ||||
chr21:44873626-44874023 | Common:8; Rare:161 | ||||
chr21:45981546-45981813 | Common:23; Rare:58; Clinvar (benign):2 | ||||
chr22:19941807-19942126 | Common:2; Rare:77 | ||||
chr22:20495787-20495994 | Common:2; Rare:77 | ||||
chr22:27919218-27919504 | Common:5; Rare:120 | ||||
chr22:30607082-30607244 | Common:2; Rare:51; Clinvar:3; Clinvar (benign):2 |