Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:122471762-122471934 | Common:3; Rare:52 | ||||
chr6:122481942-122482110 | Common:5; Rare:42 | ||||
chr6:125781059-125781134 | Rare:14 | ||||
chr6:125956651-125956886 | Common:1; Rare:66 | ||||
chr6:125986426-125986673 | Rare:105 | ||||
chr6:127266800-127266893 | Common:1; Rare:30 | ||||
chr6:127343337-127343429 | Rare:18 | ||||
chr6:128520545-128520763 | Rare:79 | ||||
chr6:131063214-131063564 | Rare:100 | ||||
chr6:131628116-131628461 | Common:3; Rare:91 | ||||
chr6:134174857-134175010 | Common:1; Rare:66 | ||||
chr6:134177843-134178014 | Rare:27 | ||||
chr6:135497705-135497890 | Common:3; Rare:75; Clinvar:1; Clinvar (benign):1 | ||||
chr6:136289767-136290014 | Common:1; Rare:107 | ||||
chr6:136550409-136550621 | Common:2; Rare:59 |