Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:27155203-27155441 | Common:7; Rare:105; Clinvar:2; Clinvar (benign):7 | ||||
chr10:27240518-27240574 | Rare:20 | ||||
chr10:27240715-27240889 | Rare:48 | ||||
chr10:27242058-27242238 | Common:1; Rare:77 | ||||
chr10:27504031-27504337 | Rare:135; Clinvar:4 | ||||
chr10:29735768-29736000 | Common:3; Rare:44 | ||||
chr10:30059529-30059634 | Rare:42 | ||||
chr10:31319021-31319237 | Common:2; Rare:67 | ||||
chr10:32056368-32056644 | Common:2; Rare:106 | ||||
chr10:32958144-32958486 | Common:2; Rare:131 | ||||
chr10:35090440-35090692 | Rare:78 | ||||
chr10:35127053-35127096 | Rare:10 | ||||
chr10:37857590-37857776 | Common:2; Rare:76 | ||||
chr10:37976544-37976798 | Rare:68 | ||||
chr10:38010530-38010746 | Common:2; Rare:101 |