Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:122451662-122452059 | Common:7; Rare:108 | ||||
chr6:123519206-123519420 | Common:1; Rare:36 | ||||
chr6:125197807-125198025 | Common:3; Rare:38 | ||||
chr6:125790047-125790254 | Common:1; Rare:38 | ||||
chr6:127267837-127268055 | Common:5; Rare:39 | ||||
chr6:129427643-129427805 | Common:1; Rare:39; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr6:129460063-129460324 | Rare:66; Clinvar:3; Clinvar (pathogenic):2 | ||||
chr6:129464994-129465244 | Common:1; Rare:57; Clinvar:1 | ||||
chr6:131689877-131689967 | Common:1; Rare:14 | ||||
chr6:134633294-134633461 | Common:1; Rare:42 | ||||
chr6:135880837-135880985 | Rare:29 | ||||
chr6:136037415-136037525 | Rare:15 | ||||
chr6:137218698-137218818 | Rare:20 | ||||
chr6:137868100-137868239 | Rare:25 | ||||
chr6:139978233-139978368 | Common:2; Rare:21 |