Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:119311793-119311939 | Common:1; Rare:17 | ||||
chr3:120615916-120616015 | Rare:22 | ||||
chr3:125087822-125088130 | Rare:61 | ||||
chr3:125109117-125109431 | Common:1; Rare:56 | ||||
chr3:128807321-128807660 | Common:1; Rare:86; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):3 | ||||
chr3:129794848-129795225 | Common:1; Rare:70 | ||||
chr3:130111410-130111777 | Common:3; Rare:94 | ||||
chr3:130112414-130112589 | Common:3; Rare:56 | ||||
chr3:140467168-140467335 | Rare:34 | ||||
chr3:141369546-141369671 | Rare:25 | ||||
chr3:149388109-149388303 | Rare:34 | ||||
chr3:150408860-150409179 | Rare:81 | ||||
chr3:153160843-153161065 | Common:2; Rare:53 | ||||
chr3:153161180-153161461 | Rare:79 | ||||
chr3:153221804-153222110 | Common:3; Rare:48 |