Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:48605010-48605210 | Common:1; Rare:53 | ||||
chr10:49538989-49539224 | Common:3; Rare:79; Clinvar:3; Clinvar (benign):2 | ||||
chr10:49941909-49942073 | Rare:46 | ||||
chr10:50067857-50068003 | Common:2; Rare:69 | ||||
chr10:50418332-50418578 | Rare:57 | ||||
chr10:50623881-50624107 | Common:1; Rare:91 | ||||
chr10:50739704-50739988 | Common:1; Rare:78 | ||||
chr10:52314073-52314419 | Common:1; Rare:83 | ||||
chr10:52314529-52314690 | Rare:58 | ||||
chr10:52315066-52315276 | Common:2; Rare:50 | ||||
chr10:56361217-56361494 | Common:6; Rare:96 | ||||
chr10:58267888-58268066 | Common:1; Rare:52 | ||||
chr10:58268924-58269231 | Common:6; Rare:88 | ||||
chr10:58512757-58513066 | Common:4; Rare:130 | ||||
chr10:58513222-58513319 | Rare:31 |