Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:53619255-53620104 | Common:3; Rare:290 | ||||
chr10:53844068-53844335 | Rare:39 | ||||
chr10:53886763-53886868 | Rare:24 | ||||
chr10:53902761-53903647 | Common:14; Rare:338; Clinvar:3; Clinvar (benign):6; Clinvar (pathogenic):3 | ||||
chr10:55467790-55468060 | Common:3; Rare:48 | ||||
chr10:55631090-55631610 | Common:8; Rare:234 | ||||
chr10:55899568-55900033 | Common:20; Rare:231 | ||||
chr10:55968870-55969270 | Common:13; Rare:67 | ||||
chr10:56132156-56132596 | Common:5; Rare:144 | ||||
chr10:56231400-56231720 | Common:7; Rare:120 | ||||
chr10:56233185-56233396 | Common:1; Rare:43 | ||||
chr10:56365070-56365325 | Common:1; Rare:42 | ||||
chr10:56554845-56555847 | Common:21; Rare:399 | ||||
chr10:56586320-56586840 | Common:5; Rare:106 | ||||
chr10:56646932-56647332 | Common:6; Rare:183 |