Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:27240861-27240964 | Common:1; Rare:21 | ||||
chr10:27241060-27241572 | Common:3; Rare:99 | ||||
chr10:27241835-27241915 | Common:1; Rare:19 | ||||
chr10:27241982-27242414 | Common:2; Rare:155 | ||||
chr10:27503969-27504185 | Common:1; Rare:54 | ||||
chr10:27504188-27504380 | Rare:109; Clinvar:3; Clinvar (benign):1 | ||||
chr10:27504476-27504781 | Rare:108 | ||||
chr10:27743112-27743257 | Common:2; Rare:49 | ||||
chr10:27998600-27998723 | Common:1; Rare:33 | ||||
chr10:28334378-28334571 | Common:1; Rare:38 | ||||
chr10:28532077-28532218 | Common:1; Rare:38 | ||||
chr10:28533676-28533865 | Common:2; Rare:67 | ||||
chr10:28534170-28534192 | Rare:3 | ||||
chr10:28534613-28534678 | Rare:15 | ||||
chr10:28677227-28677599 | Common:7; Rare:172 |