Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr9:106860004-106860174 | Rare:42 | ||||
chr9:109421341-109421528 | Rare:27 | ||||
chr9:121321102-121321401 | Common:3; Rare:73; Clinvar (benign):4 | ||||
chr9:121599330-121599692 | Common:1; Rare:97 | ||||
chr9:125238142-125238437 | Common:1; Rare:61 | ||||
chr9:126805724-126806046 | Common:1; Rare:73 | ||||
chr9:129489034-129489141 | Common:1; Rare:16 | ||||
chr9:130712994-130713045 | Rare:13 | ||||
chr9:133126326-133126491 | Common:1; Rare:22 | ||||
chr9:134413959-134414146 | Common:2; Rare:51 | ||||
chr9:135946461-135946644 | Rare:40 | ||||
chr9:135949697-135949921 | Common:1; Rare:59 | ||||
chr9:135956884-135957068 | Rare:35 | ||||
chr9:135960008-135960237 | Common:2; Rare:50 | ||||
chrM:15935-16373 |