Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:127591023-127591261 | Common:1; Rare:70 | ||||
chr7:127651848-127652253 | Common:2; Rare:118 | ||||
chr7:128409836-128410106 | Common:1; Rare:78; Clinvar:1; Clinvar (benign):1 | ||||
chr7:128455729-128455919 | Common:2; Rare:107 | ||||
chr7:128476645-128476811 | Common:1; Rare:62 | ||||
chr7:128739156-128739427 | Common:1; Rare:72 | ||||
chr7:129054878-129055234 | Common:2; Rare:67 | ||||
chr7:129611616-129611755 | Common:1; Rare:41 | ||||
chr7:130205380-130205533 | Rare:70 | ||||
chr7:131327700-131327909 | Rare:66 | ||||
chr7:134316867-134317180 | Common:2; Rare:89 | ||||
chr7:134646566-134646856 | Common:6; Rare:83 | ||||
chr7:134779290-134779743 | Rare:74 | ||||
chr7:135170440-135170538 | Rare:39 | ||||
chr7:135170598-135170892 | Common:3; Rare:104 |