Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:49539023-49539240 | Common:3; Rare:71; Clinvar:2; Clinvar (benign):2 | ||||
chr10:49941913-49942124 | Rare:64 | ||||
chr10:50067734-50067966 | Common:4; Rare:85 | ||||
chr10:50623897-50624094 | Common:1; Rare:80 | ||||
chr10:50739890-50739964 | Rare:16 | ||||
chr10:52314101-52314291 | Common:1; Rare:43 | ||||
chr10:56361214-56361459 | Common:6; Rare:82 | ||||
chr10:58385225-58385482 | Common:4; Rare:83 | ||||
chr10:60139741-60139969 | Rare:31 | ||||
chr10:60733449-60733532 | Rare:22 | ||||
chr10:62049123-62049463 | Common:2; Rare:68 | ||||
chr10:62804775-62805067 | Rare:80 | ||||
chr10:62816236-62816541 | Rare:60; Clinvar:1; Clinvar (benign):1 | ||||
chr10:62816590-62816850 | Rare:57 | ||||
chr10:63133075-63133406 | Common:2; Rare:103 |