Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:124739833-124739947 | Rare:28 | ||||
chr11:124800406-124800454 | Rare:16 | ||||
chr11:124953989-124954150 | Common:3; Rare:44 | ||||
chr11:125164540-125164755 | Rare:41 | ||||
chr11:125495388-125495595 | Common:4; Rare:73 | ||||
chr11:125496138-125496500 | Rare:78 | ||||
chr11:125592506-125592904 | Common:6; Rare:128 | ||||
chr11:125625871-125625974 | Rare:35 | ||||
chr11:125887434-125887737 | Common:2; Rare:93 | ||||
chr11:125903179-125903328 | Rare:35 | ||||
chr11:126211631-126211812 | Rare:83 | ||||
chr11:126268822-126269207 | Common:2; Rare:146; Clinvar:2; Clinvar (benign):4 | ||||
chr11:126304013-126304070 | Rare:29 | ||||
chr11:126304239-126304397 | Common:3; Rare:60 | ||||
chr11:126355532-126355825 | Common:1; Rare:76 |