Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:27100427-27100586 | Common:3; Rare:48; Clinvar:4; Clinvar (benign):2 | ||||
chr10:27154314-27154486 | Rare:47 | ||||
chr10:27155241-27155390 | Common:3; Rare:52; Clinvar:2; Clinvar (benign):3 | ||||
chr10:27240445-27240536 | Rare:32 | ||||
chr10:27240564-27240896 | Common:2; Rare:85 | ||||
chr10:27242058-27242237 | Common:1; Rare:76 | ||||
chr10:27504132-27504367 | Rare:123; Clinvar:4; Clinvar (benign):1 | ||||
chr10:28532480-28532815 | Common:5; Rare:133 | ||||
chr10:29634913-29635132 | Common:1; Rare:44 | ||||
chr10:29735768-29735994 | Common:3; Rare:42 | ||||
chr10:29736936-29737131 | Common:2; Rare:58 | ||||
chr10:30059501-30059651 | Common:1; Rare:58 | ||||
chr10:30349271-30349399 | Common:12; Rare:77 | ||||
chr10:31031838-31032039 | Common:2; Rare:79 | ||||
chr10:31318683-31318835 | Common:1; Rare:48 |