Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:102642129-102642356 | Common:1; Rare:59 | ||||
chr10:102642639-102642953 | Common:1; Rare:85 | ||||
chr10:102878673-102878891 | Common:1; Rare:45 | ||||
chr10:102919642-102919783 | Rare:25 | ||||
chr10:103097334-103097543 | Common:3; Rare:45 | ||||
chr10:103098935-103099147 | Common:2; Rare:39; Clinvar (benign):1 | ||||
chr10:103102071-103102232 | Rare:19 | ||||
chr10:103517398-103517546 | Common:2; Rare:26 | ||||
chr10:103659890-103660188 | Common:2; Rare:58 | ||||
chr10:103661663-103661961 | Common:1; Rare:89 | ||||
chr10:103668729-103668840 | Rare:34 | ||||
chr10:103706854-103707050 | Common:2; Rare:39 | ||||
chr10:103898399-103898504 | Rare:15 | ||||
chr10:104162316-104162617 | Common:2; Rare:57 | ||||
chr10:104665805-104665883 | Rare:13 |