Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:197949894-197950250 | Common:4; Rare:110; Clinvar (benign):2 | ||||
chr3:197959989-197960248 | Common:1; Rare:91 | ||||
chr4:499149-499261 | Common:2; Rare:33 | ||||
chr4:674223-674560 | Common:1; Rare:159 | ||||
chr4:932300-932487 | Common:2; Rare:76 | ||||
chr4:2468886-2469148 | Common:2; Rare:94 | ||||
chr4:2843709-2843977 | Common:3; Rare:93 | ||||
chr4:2934788-2934903 | Common:1; Rare:55 | ||||
chr4:4290121-4290282 | Common:3; Rare:63 | ||||
chr4:4541945-4542158 | Common:1; Rare:89 | ||||
chr4:6640541-6640720 | Common:2; Rare:74 | ||||
chr4:6693685-6693875 | Rare:36 | ||||
chr4:6987028-6987268 | Common:1; Rare:72 | ||||
chr4:8440723-8441006 | Rare:108 | ||||
chr4:10116712-10117103 | Common:8; Rare:191 |