Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:102418723-102418995 | Rare:61 | ||||
chr10:102419449-102419943 | Common:1; Rare:188 | ||||
chr10:102420704-102420866 | Rare:32 | ||||
chr10:102420896-102421213 | Rare:114 | ||||
chr10:102432510-102432759 | Common:1; Rare:69 | ||||
chr10:102461230-102461454 | Rare:64 | ||||
chr10:102502027-102502362 | Common:3; Rare:101 | ||||
chr10:102502650-102503063 | Common:2; Rare:216 | ||||
chr10:102503694-102504039 | Common:4; Rare:94; Clinvar:1; Clinvar (benign):1 | ||||
chr10:102714151-102714694 | Common:3; Rare:168 | ||||
chr10:102743738-102743991 | Common:2; Rare:65 | ||||
chr10:102775752-102776013 | Rare:45 | ||||
chr10:102776078-102776371 | Common:1; Rare:64 | ||||
chr10:102854061-102854295 | Common:1; Rare:78 | ||||
chr10:102854460-102854631 | Common:1; Rare:42 |