Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:123509754-123509946 | Rare:46 | ||||
chr11:123654562-123654763 | Common:5; Rare:52; Clinvar (benign):1 | ||||
chr11:123741631-123741812 | Common:1; Rare:56 | ||||
chr11:124622271-124622671 | Common:5; Rare:105 | ||||
chr11:124622684-124622922 | Common:5; Rare:81 | ||||
chr11:124673706-124673944 | Common:4; Rare:73 | ||||
chr11:124739770-124739969 | Rare:61 | ||||
chr11:124800334-124800514 | Common:1; Rare:74 | ||||
chr11:124876727-124876915 | Common:3; Rare:39 | ||||
chr11:124953885-124954215 | Common:5; Rare:95 | ||||
chr11:125062782-125063182 | Common:5; Rare:109 | ||||
chr11:125110960-125111621 | Common:7; Rare:205 | ||||
chr11:125111813-125112041 | Common:2; Rare:50 | ||||
chr11:125164527-125164915 | Rare:83 | ||||
chr11:125451461-125451634 | Rare:39 |