Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:55947916-55948228 | Common:2; Rare:54 | ||||
chr4:56410292-56410509 | Common:1; Rare:41 | ||||
chr4:56491314-56491567 | Rare:62; Clinvar (benign):1 | ||||
chr4:68337307-68337632 | Common:1; Rare:96 | ||||
chr4:76306583-76306772 | Rare:61 | ||||
chr4:76738404-76738715 | Rare:58 | ||||
chr4:77033005-77033124 | Rare:17 | ||||
chr4:77048589-77048911 | Common:3; Rare:91 | ||||
chr4:77058510-77058785 | Common:3; Rare:62 | ||||
chr4:77066283-77066599 | Common:2; Rare:77 | ||||
chr4:78182055-78182296 | Common:1; Rare:51 | ||||
chr4:84965546-84965660 | Common:1; Rare:30 | ||||
chr4:87980119-87980426 | Rare:54 | ||||
chr4:90839105-90839355 | Common:1; Rare:46 | ||||
chr4:110476615-110476838 | Rare:92 |