Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:151408861-151409156 | Common:5; Rare:94 | ||||
chr4:152779691-152780013 | Common:1; Rare:88 | ||||
chr4:153204267-153204502 | Common:2; Rare:47 | ||||
chr4:158173023-158173079 | Rare:12 | ||||
chr4:158671830-158672313 | Common:5; Rare:121; Clinvar:2; Clinvar (benign):1 | ||||
chr4:158723314-158723463 | Common:2; Rare:66 | ||||
chr4:168480476-168480574 | Rare:13 | ||||
chr4:169270971-169271307 | Common:2; Rare:104 | ||||
chr4:169620335-169620598 | Common:2; Rare:102 | ||||
chr4:173530195-173530353 | Rare:33 | ||||
chr4:174283322-174283332 | Rare:2 | ||||
chr4:174283618-174283938 | Common:1; Rare:62 | ||||
chr4:174284262-174284392 | Common:1; Rare:29 | ||||
chr4:174522399-174522613 | Rare:69; Clinvar:2; Clinvar (pathogenic):1 | ||||
chr4:177442377-177442514 | Rare:82; Clinvar:2 |