Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:27032867-27033009 | Rare:53 | ||||
chr2:27051546-27051689 | Rare:43 | ||||
chr2:27071525-27071871 | Common:1; Rare:105 | ||||
chr2:27211739-27212057 | Common:3; Rare:110 | ||||
chr2:27212223-27212378 | Common:1; Rare:82 | ||||
chr2:27217115-27217452 | Common:1; Rare:108 | ||||
chr2:27323043-27323154 | Rare:27; Clinvar (benign):1 | ||||
chr2:27356743-27356863 | Rare:32 | ||||
chr2:27356961-27357170 | Common:2; Rare:72 | ||||
chr2:27370275-27370674 | Common:1; Rare:164 | ||||
chr2:27582797-27583101 | Rare:103 | ||||
chr2:27628939-27629127 | Common:1; Rare:102 | ||||
chr2:27663369-27663490 | Rare:30 | ||||
chr2:27663503-27663928 | Rare:146 | ||||
chr2:27771634-27771771 | Common:1; Rare:52 |