Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:70086931-70087114 | Common:1; Rare:92 | ||||
chr2:70258033-70258242 | Common:2; Rare:74 | ||||
chr2:70293645-70293902 | Common:3; Rare:84 | ||||
chr2:71068538-71068698 | Rare:69 | ||||
chr2:71130210-71130677 | Common:6; Rare:133; Clinvar:1; Clinvar (benign):2 | ||||
chr2:71453515-71453907 | Common:2; Rare:74 | ||||
chr2:73071701-73071841 | Common:2; Rare:54 | ||||
chr2:73234176-73234375 | Common:2; Rare:61 | ||||
chr2:73385620-73385866 | Common:2; Rare:94; Clinvar:7; Clinvar (benign):3 | ||||
chr2:73386021-73386081 | Rare:32; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr2:73828804-73829029 | Common:1; Rare:53 | ||||
chr2:73892652-73893470 | Common:5; Rare:168 | ||||
chr2:74147830-74148161 | Common:3; Rare:87; Clinvar:2; Clinvar (benign):1 | ||||
chr2:74178752-74179065 | Common:3; Rare:89 | ||||
chr2:74391793-74391941 | Common:1; Rare:91 |