Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr9:121074842-121074967 | Rare:59 | ||||
chr9:121201814-121202149 | Common:2; Rare:105 | ||||
chr9:121285821-121286150 | Common:2; Rare:66 | ||||
chr9:121370213-121370512 | Common:1; Rare:86 | ||||
chr9:121566849-121567133 | Rare:68 | ||||
chr9:122159696-122159908 | Rare:86 | ||||
chr9:122264748-122264923 | Common:2; Rare:50 | ||||
chr9:122931482-122931694 | Common:3; Rare:44 | ||||
chr9:124861890-124862121 | Rare:100 | ||||
chr9:124940969-124941156 | Common:3; Rare:62 | ||||
chr9:125189733-125190029 | Common:1; Rare:139 | ||||
chr9:125241350-125241686 | Common:2; Rare:92 | ||||
chr9:125261728-125261841 | Common:1; Rare:40 | ||||
chr9:127449614-127449989 | Rare:98 | ||||
chr9:127451263-127451565 | Common:3; Rare:125; Clinvar (benign):1 |