Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:87760158-87760369 | Rare:41 | ||||
chr10:87769855-87769924 | Common:2; Rare:9 | ||||
chr10:87775450-87775507 | Rare:14 | ||||
chr10:87862249-87862588 | Rare:163; Clinvar:1 | ||||
chr10:87865015-87865296 | Rare:52 | ||||
chr10:87865636-87865873 | Rare:43 | ||||
chr10:87865983-87866205 | Common:1; Rare:40 | ||||
chr10:87876944-87877209 | Rare:33 | ||||
chr10:88492167-88492391 | Common:1; Rare:35 | ||||
chr10:88988295-88988415 | Common:1; Rare:19 | ||||
chr10:89115264-89115470 | Common:1; Rare:31 | ||||
chr10:89225139-89225340 | Common:2; Rare:65; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
chr10:89456543-89456795 | Rare:46 | ||||
chr10:90900387-90900678 | Rare:75 | ||||
chr10:90908274-90908290 | Rare:2 |