Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:150581723-150581934 | Rare:41 | ||||
chr4:151015239-151015439 | Rare:52 | ||||
chr4:151099327-151099709 | Common:3; Rare:122 | ||||
chr4:151100241-151100587 | Common:1; Rare:67 | ||||
chr4:151409025-151409188 | Common:3; Rare:45 | ||||
chr4:152779667-152780013 | Common:2; Rare:93 | ||||
chr4:153788610-153788710 | Common:2; Rare:27 | ||||
chr4:153788922-153789188 | Rare:79 | ||||
chr4:154550372-154550504 | Rare:41 | ||||
chr4:156971124-156971183 | Rare:8 | ||||
chr4:158172360-158172435 | Rare:14 | ||||
chr4:158672044-158672321 | Common:3; Rare:62; Clinvar:2; Clinvar (benign):1 | ||||
chr4:164977625-164977646 | Rare:4 | ||||
chr4:169620385-169620673 | Common:2; Rare:105 | ||||
chr4:169660036-169660254 | Common:1; Rare:41 |