Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:22325520-22325856 | Rare:135 | ||||
chr10:24208812-24209178 | Rare:102 | ||||
chr10:24466416-24466505 | Rare:12 | ||||
chr10:24722742-24722836 | Rare:33 | ||||
chr10:25015946-25016227 | Common:2; Rare:71 | ||||
chr10:25016435-25016671 | Common:8; Rare:87 | ||||
chr10:25016946-25017121 | Common:4; Rare:78 | ||||
chr10:25174432-25174771 | Rare:67 | ||||
chr10:26697565-26697927 | Common:2; Rare:109; Clinvar:2; Clinvar (benign):3 | ||||
chr10:27100432-27100610 | Common:3; Rare:50; Clinvar:4; Clinvar (benign):2 | ||||
chr10:27154254-27154480 | Rare:61 | ||||
chr10:27155163-27155426 | Common:7; Rare:111; Clinvar:5; Clinvar (benign):7 | ||||
chr10:27240478-27240667 | Common:2; Rare:58 | ||||
chr10:27240741-27240874 | Rare:36 | ||||
chr10:27242058-27242245 | Common:1; Rare:82 |