Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:179806884-179807056 | Common:3; Rare:64 | ||||
chr5:179820704-179821030 | Common:6; Rare:125; Clinvar:3; Clinvar (benign):2 | ||||
chr5:179823969-179824243 | Common:1; Rare:110; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr5:179858797-179859026 | Rare:120 | ||||
chr5:180802772-180802958 | Common:6; Rare:77 | ||||
chr5:180810102-180810223 | Common:1; Rare:26 | ||||
chr5:180861210-180861598 | Common:4; Rare:128 | ||||
chr5:181040110-181040293 | Rare:35 | ||||
chr5:181223102-181223328 | Rare:83 | ||||
chr5:181223529-181223814 | Common:4; Rare:68 | ||||
chr5:181243680-181243875 | Common:2; Rare:62 | ||||
chr5:181261054-181261280 | Rare:78 | ||||
chr6:693061-693194 | Rare:43 | ||||
chr6:2245442-2245833 | Common:1; Rare:133 | ||||
chr6:2971269-2971484 | Common:4; Rare:54 |