Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:46617025-46617270 | Common:7; Rare:109 | ||||
chr2:46915722-46915910 | Common:1; Rare:57; Clinvar:2; Clinvar (benign):1 | ||||
chr2:46941715-46941764 | Common:1; Rare:18; Clinvar (benign):1 | ||||
chr2:47176439-47176750 | Common:3; Rare:153; Clinvar (benign):5 | ||||
chr2:53767618-53767866 | Common:3; Rare:84 | ||||
chr2:53786839-53787191 | Common:1; Rare:137 | ||||
chr2:53970788-53971126 | Common:10; Rare:113 | ||||
chr2:54456094-54456421 | Common:1; Rare:123 | ||||
chr2:55050205-55050238 | Rare:8 | ||||
chr2:55050267-55050429 | Common:1; Rare:61 | ||||
chr2:55050432-55050747 | Common:4; Rare:96 | ||||
chr2:55232241-55232375 | Common:2; Rare:31 | ||||
chr2:55519432-55519746 | Common:1; Rare:84 | ||||
chr2:55923664-55924018 | Common:5; Rare:122; Clinvar:2; Clinvar (benign):9 | ||||
chr2:58046613-58046717 | Rare:32 |