Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:102401876-102402292 | Common:3; Rare:126; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr10:102643272-102643428 | Common:3; Rare:33 | ||||
chr10:103696667-103696771 | Rare:21 | ||||
chr10:110395964-110396280 | Common:1; Rare:57 | ||||
chr10:110496212-110496502 | Common:2; Rare:68 | ||||
chr10:110507171-110507493 | Rare:71 | ||||
chr10:110509970-110510077 | Rare:27 | ||||
chr10:110583875-110584327 | Common:3; Rare:94; Clinvar (benign):2 | ||||
chr10:110598122-110598156 | Rare:4 | ||||
chr10:110604011-110604200 | Rare:45 | ||||
chr10:110947532-110947618 | Rare:22 | ||||
chr10:113013141-113013444 | Common:2; Rare:52 | ||||
chr10:113079131-113079192 | Rare:8 | ||||
chr10:113086412-113086686 | Rare:51 | ||||
chr10:113088078-113088128 | Rare:8 |