Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:124673710-124673929 | Common:4; Rare:68 | ||||
chr11:124762287-124762439 | Rare:38 | ||||
chr11:124876653-124876869 | Common:2; Rare:47 | ||||
chr11:125164558-125164754 | Rare:37 | ||||
chr11:125496235-125496466 | Rare:49 | ||||
chr11:125592520-125592930 | Common:6; Rare:134 | ||||
chr11:125625875-125625935 | Rare:23 | ||||
chr11:126211641-126211812 | Rare:79 | ||||
chr11:126268829-126269186 | Common:1; Rare:133; Clinvar:2; Clinvar (benign):2 | ||||
chr11:126303974-126304082 | Rare:62 | ||||
chr11:126355531-126355763 | Common:1; Rare:65 | ||||
chr11:130314417-130314521 | Common:1; Rare:34 | ||||
chr11:130916421-130916663 | Common:5; Rare:74 | ||||
chr11:134253292-134253586 | Common:2; Rare:99; Clinvar (benign):1 | ||||
chr12:389256-389360 | Rare:35 |