Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:124730359-124730464 | Common:3; Rare:56; Clinvar:1; Clinvar (benign):3 | ||||
chr3:127598209-127598458 | Common:3; Rare:73 | ||||
chr3:128052170-128052473 | Common:2; Rare:101 | ||||
chr3:128879408-128879665 | Common:4; Rare:121; Clinvar:2; Clinvar (benign):2 | ||||
chr3:129183814-129184108 | Common:2; Rare:109 | ||||
chr3:129439876-129440254 | Common:1; Rare:111; Clinvar:1; Clinvar (benign):1 | ||||
chr3:134485442-134485772 | Rare:81 | ||||
chr3:134485969-134486208 | Common:2; Rare:78 | ||||
chr3:136861995-136862269 | Common:1; Rare:84 | ||||
chr3:139389608-139389851 | Common:1; Rare:77 | ||||
chr3:143001436-143001625 | Common:3; Rare:69 | ||||
chr3:146160982-146161271 | Common:1; Rare:97; Clinvar:4; Clinvar (benign):2 | ||||
chr3:149129549-149129718 | Common:1; Rare:71; Clinvar:2; Clinvar (benign):1 | ||||
chr3:149377640-149377781 | Common:1; Rare:37 | ||||
chr3:150603168-150603367 | Common:2; Rare:80 |