Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:125625871-125625990 | Rare:39 | ||||
chr11:125887480-125887737 | Common:2; Rare:82 | ||||
chr11:126062717-126063014 | Common:7; Rare:101 | ||||
chr11:126211623-126211812 | Rare:87 | ||||
chr11:126268785-126269198 | Common:1; Rare:157; Clinvar:2; Clinvar (benign):3 | ||||
chr11:126303974-126304112 | Rare:84 | ||||
chr11:126355526-126355763 | Common:2; Rare:66 | ||||
chr11:128522247-128522540 | Common:1; Rare:86 | ||||
chr11:128692847-128693001 | Rare:39 | ||||
chr11:128693797-128694099 | Common:2; Rare:52 | ||||
chr11:129895517-129895675 | Common:2; Rare:64 | ||||
chr11:130002823-130002953 | Rare:28 | ||||
chr11:130069532-130070049 | Common:2; Rare:192 | ||||
chr11:130314414-130314497 | Common:1; Rare:23 | ||||
chr11:130448465-130448687 | Common:1; Rare:53 |