Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:102399572-102399817 | Rare:68; Clinvar (benign):1 | ||||
chr10:102422218-102422416 | Rare:37 | ||||
chr10:102422695-102422913 | Rare:59 | ||||
chr10:102431835-102431989 | Common:2; Rare:27 | ||||
chr10:102449686-102449880 | Common:1; Rare:36 | ||||
chr10:102450332-102450732 | Common:1; Rare:175 | ||||
chr10:102450804-102450954 | Rare:46 | ||||
chr10:102453076-102453198 | Rare:22 | ||||
chr10:102463482-102463640 | Rare:19 | ||||
chr10:102596551-102596731 | Common:1; Rare:19 | ||||
chr10:102604461-102604680 | Common:1; Rare:37 | ||||
chr10:102605588-102605988 | Common:4; Rare:87 | ||||
chr10:102642092-102642356 | Common:1; Rare:68 | ||||
chr10:102642807-102642950 | Common:1; Rare:28 | ||||
chr10:102643184-102643435 | Common:3; Rare:55 |