Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:27086587-27086773 | Rare:54 | ||||
chr2:27211924-27212109 | Common:3; Rare:71 | ||||
chr2:27212280-27212437 | Common:2; Rare:81 | ||||
chr2:27323045-27323116 | Rare:16; Clinvar (benign):1 | ||||
chr2:27356743-27357170 | Common:2; Rare:123 | ||||
chr2:27370247-27370633 | Common:1; Rare:156 | ||||
chr2:27583010-27583104 | Rare:36 | ||||
chr2:27628977-27629058 | Common:1; Rare:41 | ||||
chr2:27663395-27663440 | Rare:11 | ||||
chr2:27663560-27663911 | Rare:126 | ||||
chr2:27890406-27890829 | Rare:109 | ||||
chr2:28392633-28392893 | Rare:93 | ||||
chr2:28395401-28395735 | Common:2; Rare:65 | ||||
chr2:28751695-28752172 | Common:2; Rare:200 | ||||
chr2:28870262-28870418 | Rare:61 |