Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:136944669-136944848 | Rare:35 | ||||
chr7:136950775-136950947 | Common:3; Rare:39 | ||||
chr7:136951896-136952154 | Common:1; Rare:44 | ||||
chr7:136962925-136963005 | Common:1; Rare:8 | ||||
chr7:136967327-136967514 | Common:1; Rare:34 | ||||
chr7:136992070-136992265 | Common:3; Rare:27; Clinvar (benign):3 | ||||
chr7:137000630-137000716 | Rare:10 | ||||
chr7:137001514-137001680 | Rare:25 | ||||
chr7:137004870-137005097 | Common:2; Rare:36 | ||||
chr7:137009957-137010188 | Common:1; Rare:35 | ||||
chr7:137078590-137078757 | Rare:27 | ||||
chr7:137092059-137092161 | Common:1; Rare:11 | ||||
chr7:137283619-137283937 | Common:1; Rare:57 | ||||
chr7:137342941-137343140 | Rare:27 | ||||
chr7:137721776-137721980 | Rare:32 |