Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:116574806-116574938 | Common:2; Rare:46 | ||||
chr5:118988194-118988292 | Rare:42 | ||||
chr5:119070879-119071207 | Common:3; Rare:104 | ||||
chr5:119268604-119268840 | Common:1; Rare:63 | ||||
chr5:119355809-119356100 | Common:5; Rare:85 | ||||
chr5:121961821-121962062 | Common:2; Rare:91 | ||||
chr5:122077107-122077334 | Common:1; Rare:45 | ||||
chr5:122845516-122845639 | Common:3; Rare:48 | ||||
chr5:123036533-123036802 | Common:1; Rare:81 | ||||
chr5:123511981-123512280 | Common:1; Rare:81 | ||||
chr5:124748791-124749019 | Common:3; Rare:56 | ||||
chr5:126423324-126423594 | Rare:76 | ||||
chr5:126595167-126595327 | Common:2; Rare:77; Clinvar:5; Clinvar (benign):7 | ||||
chr5:126776844-126777175 | Common:3; Rare:127; Clinvar:4; Clinvar (benign):5 | ||||
chr5:126811592-126811802 | Common:2; Rare:39 |