Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:71851112-71851514 | Common:5; Rare:146; Clinvar:5; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
chr10:71964075-71964096 | Rare:3 | ||||
chr10:71964196-71964558 | Common:4; Rare:98; Clinvar:1; Clinvar (benign):3 | ||||
chr10:71964586-71965018 | Common:2; Rare:101; Clinvar:1 | ||||
chr10:72215859-72216157 | Rare:107 | ||||
chr10:72216212-72216413 | Rare:78 | ||||
chr10:72216421-72216448 | Rare:5 | ||||
chr10:72273348-72273434 | Rare:16 | ||||
chr10:72273454-72274161 | Common:3; Rare:182 | ||||
chr10:72274400-72274704 | Common:2; Rare:88 | ||||
chr10:72336372-72336556 | Rare:39 | ||||
chr10:72336791-72336947 | Common:1; Rare:40 | ||||
chr10:72337197-72337272 | Rare:14 | ||||
chr10:72353632-72353889 | Common:2; Rare:48 | ||||
chr10:72354145-72354202 | Rare:11 |