Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:125719453-125719820 | Common:1; Rare:137 | ||||
chr10:125823200-125823607 | Common:1; Rare:142; Clinvar:1; Clinvar (benign):1 | ||||
chr10:125896284-125896629 | Common:5; Rare:30 | ||||
chr10:126905297-126905484 | Rare:75 | ||||
chr10:127892602-127892960 | Rare:109 | ||||
chr10:128047411-128047635 | Common:2; Rare:74 | ||||
chr10:132331806-132332311 | Common:15; Rare:164 | ||||
chr10:133308829-133308989 | Rare:75 | ||||
chr10:133309162-133309415 | Common:2; Rare:93 | ||||
chr10:133357990-133358291 | Common:8; Rare:73 | ||||
chr10:133373295-133373481 | Common:2; Rare:76; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
chr11:207333-207726 | Common:8; Rare:131 | ||||
chr11:208615-208884 | Rare:97 | ||||
chr11:236324-236563 | Common:8; Rare:82 | ||||
chr11:236917-237073 | Common:1; Rare:62 |