Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:124953986-124954202 | Common:4; Rare:60 | ||||
chr11:125111712-125111990 | Common:3; Rare:57 | ||||
chr11:125592520-125592908 | Common:6; Rare:126 | ||||
chr11:125887460-125887730 | Common:2; Rare:82 | ||||
chr11:126211596-126211807 | Rare:100 | ||||
chr11:126268776-126269209 | Common:2; Rare:167; Clinvar:2; Clinvar (benign):4 | ||||
chr11:126303979-126304133 | Rare:95 | ||||
chr11:126355548-126355777 | Rare:61 | ||||
chr11:130069665-130069946 | Common:2; Rare:95 | ||||
chr11:130448474-130448647 | Rare:45 | ||||
chr11:134223941-134224156 | Common:1; Rare:66 | ||||
chr11:134253292-134253601 | Common:2; Rare:108; Clinvar (benign):1 | ||||
chr12:389271-389364 | Rare:29 | ||||
chr12:401446-401666 | Rare:58 | ||||
chr12:991113-991243 | Common:1; Rare:49 |