Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:42199019-42199181 | Rare:35 | ||||
chr2:43888674-43888966 | Common:3; Rare:79 | ||||
chr2:43889897-43889958 | Common:2; Rare:13 | ||||
chr2:43890218-43890482 | Common:2; Rare:91 | ||||
chr2:43949523-43949654 | Rare:50; Clinvar (pathogenic):2 | ||||
chr2:43973606-43973855 | Rare:88; Clinvar:6; Clinvar (benign):3 | ||||
chr2:43990638-43990788 | Common:1; Rare:28 | ||||
chr2:46587466-46587591 | Common:2; Rare:20 | ||||
chr2:46643653-46643898 | Common:1; Rare:53 | ||||
chr2:46770720-46770957 | Common:2; Rare:54 | ||||
chr2:47162285-47162698 | Rare:72; Clinvar (benign):4 | ||||
chr2:47165383-47165631 | Common:2; Rare:65 | ||||
chr2:47171815-47171888 | Rare:10 | ||||
chr2:47174911-47175134 | Common:4; Rare:69 | ||||
chr2:47175516-47175718 | Rare:72 |