Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:152779730-152780160 | Common:2; Rare:112 | ||||
chr4:156971073-156971190 | Rare:19 | ||||
chr4:158173023-158173064 | Rare:11 | ||||
chr4:158210305-158210567 | Common:3; Rare:63 | ||||
chr4:158671866-158672359 | Common:5; Rare:116; Clinvar:2; Clinvar (benign):1 | ||||
chr4:158723348-158723439 | Rare:42 | ||||
chr4:163166832-163166963 | Common:2; Rare:41 | ||||
chr4:165112818-165112973 | Rare:46 | ||||
chr4:169010237-169010452 | Common:1; Rare:60 | ||||
chr4:169270939-169271168 | Common:1; Rare:75 | ||||
chr4:169620360-169620707 | Common:2; Rare:123 | ||||
chr4:173168028-173168272 | Common:3; Rare:45 | ||||
chr4:173168686-173168831 | Common:2; Rare:56 | ||||
chr4:173530197-173530356 | Rare:33 | ||||
chr4:174283618-174283938 | Common:1; Rare:62 |