Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:72135570-72135837 | Common:5; Rare:54 | ||||
chr11:72223762-72223927 | Rare:46 | ||||
chr11:72228947-72229246 | Rare:79; Clinvar (pathogenic):1 | ||||
chr11:72579328-72579572 | Common:1; Rare:69 | ||||
chr11:72584303-72584623 | Common:3; Rare:105 | ||||
chr11:72589912-72590230 | Common:1; Rare:80 | ||||
chr11:72636021-72636193 | Rare:54 | ||||
chr11:72695694-72696035 | Rare:78 | ||||
chr11:72703360-72703610 | Common:4; Rare:60 | ||||
chr11:72722196-72722658 | Rare:105 | ||||
chr11:72752345-72752530 | Common:2; Rare:61 | ||||
chr11:72793655-72793832 | Common:1; Rare:51 | ||||
chr11:72814020-72814046 | Common:2; Rare:10 | ||||
chr11:72814054-72814535 | Common:4; Rare:145 | ||||
chr11:73141223-73141493 | Rare:70 |