Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr9:122905281-122905431 | Common:1; Rare:79 | ||||
chr9:122931482-122931680 | Common:3; Rare:36 | ||||
chr9:124861494-124861768 | Common:3; Rare:84 | ||||
chr9:124861883-124862125 | Rare:107 | ||||
chr9:124940969-124941150 | Common:3; Rare:62 | ||||
chr9:125189733-125190039 | Common:1; Rare:140 | ||||
chr9:125241366-125241669 | Common:1; Rare:80 | ||||
chr9:125261702-125261848 | Common:1; Rare:55 | ||||
chr9:125707184-125707364 | Common:2; Rare:54 | ||||
chr9:126804869-126805046 | Common:1; Rare:56 | ||||
chr9:127451257-127451557 | Common:3; Rare:127; Clinvar (benign):1 | ||||
chr9:127899525-127899819 | Common:2; Rare:93 | ||||
chr9:127937816-127938012 | Common:2; Rare:52; Clinvar:4; Clinvar (benign):2 | ||||
chr9:128160024-128160401 | Common:2; Rare:89 | ||||
chr9:128191515-128191651 | Rare:35 |