Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:121696885-121697130 | Common:5; Rare:70 | ||||
chr4:122922933-122923101 | Common:2; Rare:41 | ||||
chr4:127880778-127880929 | Rare:53 | ||||
chr4:128061002-128061325 | Common:1; Rare:116 | ||||
chr4:129093492-129093741 | Rare:76 | ||||
chr4:133149085-133149316 | Common:2; Rare:68 | ||||
chr4:137532450-137532637 | Rare:30 | ||||
chr4:139453729-139454256 | Common:3; Rare:153; Clinvar:10; Clinvar (benign):4 | ||||
chr4:139556154-139556298 | Rare:32 | ||||
chr4:140373384-140373680 | Common:2; Rare:113 | ||||
chr4:143336875-143337180 | Common:1; Rare:101 | ||||
chr4:143513349-143513541 | Common:2; Rare:70 | ||||
chr4:145098156-145098348 | Rare:69 | ||||
chr4:145619272-145619406 | Rare:59; Clinvar:2; Clinvar (benign):1 | ||||
chr4:147684133-147684292 | Rare:63 |