Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:130342332-130342440 | Common:1; Rare:25 | ||||
chr2:130342642-130342930 | Common:5; Rare:90 | ||||
chr2:130756027-130756370 | Common:3; Rare:121 | ||||
chr2:131093309-131093597 | Common:1; Rare:124 | ||||
chr2:131105193-131105368 | Common:1; Rare:79 | ||||
chr2:131492310-131492438 | Common:3; Rare:56 | ||||
chr2:131492701-131492959 | Common:4; Rare:80 | ||||
chr2:131493034-131493140 | Common:1; Rare:30 | ||||
chr2:132670171-132670468 | Common:1; Rare:67 | ||||
chr2:134918209-134918298 | Common:1; Rare:25 | ||||
chr2:134918580-134918894 | Common:1; Rare:130 | ||||
chr2:135052162-135052314 | Common:1; Rare:53; Clinvar (benign):1 | ||||
chr2:135530706-135530960 | Common:3; Rare:59 | ||||
chr2:135531172-135531621 | Common:1; Rare:100 | ||||
chr2:135586212-135586451 | Rare:45 |