Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:37849298-37849480 | Rare:107 | ||||
chr22:38201749-38202000 | Rare:78 | ||||
chr22:38505992-38506108 | Common:1; Rare:44 | ||||
chr22:38506299-38506619 | Common:1; Rare:97 | ||||
chr22:38570184-38570406 | Common:2; Rare:38 | ||||
chr22:38656382-38656687 | Common:1; Rare:72 | ||||
chr22:38681832-38682009 | Common:1; Rare:77 | ||||
chr22:38957410-38957612 | Rare:39 | ||||
chr22:39040756-39040891 | Common:1; Rare:33 | ||||
chr22:39319596-39319839 | Common:3; Rare:101 | ||||
chr22:39502141-39502379 | Rare:65 | ||||
chr22:40346445-40346556 | Rare:47; Clinvar:2; Clinvar (benign):2 | ||||
chr22:40636651-40636982 | Common:2; Rare:97 | ||||
chr22:40819312-40819506 | Common:11; Rare:101 | ||||
chr22:40856573-40857154 | Common:2; Rare:226; Clinvar:3 |