Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:38751266-38751616 | Common:5; Rare:188 | ||||
chr2:38875886-38876105 | Common:1; Rare:78 | ||||
chr2:39120992-39121141 | Rare:56 | ||||
chr2:39436983-39437464 | Common:5; Rare:181 | ||||
chr2:40511950-40512027 | Rare:12 | ||||
chr2:42169182-42169565 | Common:1; Rare:176 | ||||
chr2:42169568-42169627 | Common:2; Rare:29 | ||||
chr2:42792529-42792849 | Common:3; Rare:94 | ||||
chr2:43226161-43226351 | Rare:80 | ||||
chr2:43226554-43226837 | Common:2; Rare:116 | ||||
chr2:43595940-43596205 | Common:1; Rare:96 | ||||
chr2:43774391-43774434 | Rare:7 | ||||
chr2:43995960-43996281 | Common:4; Rare:140; Clinvar:1; Clinvar (benign):1 | ||||
chr2:44361469-44362007 | Common:3; Rare:170 | ||||
chr2:46297204-46297466 | Common:4; Rare:89; Clinvar:1; Clinvar (benign):1 |