Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:27071545-27071960 | Common:2; Rare:116 | ||||
chr2:27078783-27078921 | Common:1; Rare:23 | ||||
chr2:27211935-27212072 | Common:3; Rare:52 | ||||
chr2:27212280-27212370 | Common:1; Rare:43 | ||||
chr2:27323045-27323136 | Rare:21; Clinvar (benign):1 | ||||
chr2:27356746-27356854 | Rare:26 | ||||
chr2:27356968-27357077 | Rare:43 | ||||
chr2:27370316-27370677 | Common:1; Rare:142 | ||||
chr2:27582982-27583095 | Rare:40 | ||||
chr2:27628959-27629060 | Common:1; Rare:52 | ||||
chr2:27663578-27663911 | Rare:119 | ||||
chr2:27890425-27890803 | Rare:94 | ||||
chr2:28751726-28752134 | Common:1; Rare:168 | ||||
chr2:28870269-28870437 | Rare:60 | ||||
chr2:32039761-32039851 | Rare:27 |