Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:52685942-52686043 | Common:1; Rare:33 | ||||
chr3:52705583-52706181 | Common:4; Rare:191 | ||||
chr3:52843196-52843497 | Common:3; Rare:65 | ||||
chr3:53347513-53347730 | Common:2; Rare:70 | ||||
chr3:53846407-53846575 | Rare:56 | ||||
chr3:53891794-53892021 | Common:2; Rare:71 | ||||
chr3:56557081-56557228 | Common:2; Rare:55 | ||||
chr3:57079252-57079388 | Common:2; Rare:45 | ||||
chr3:57227604-57227922 | Common:4; Rare:106 | ||||
chr3:57555996-57556331 | Rare:83 | ||||
chr3:57597314-57597661 | Common:4; Rare:109 | ||||
chr3:57692957-57693172 | Common:1; Rare:66 | ||||
chr3:58149910-58150217 | Rare:108; Clinvar:2; Clinvar (benign):3 | ||||
chr3:58433799-58433997 | Common:1; Rare:77; Clinvar (benign):3 | ||||
chr3:58577311-58577736 | Common:2; Rare:69 |