Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:116571202-116571595 | Common:3; Rare:111 | ||||
chr6:118547999-118548362 | Common:2; Rare:72; Clinvar:3; Clinvar (benign):2 | ||||
chr6:118893885-118894200 | Common:3; Rare:98 | ||||
chr6:119349630-119349930 | Common:3; Rare:99 | ||||
chr6:121334457-121334531 | Common:2; Rare:26 | ||||
chr6:121334698-121334855 | Common:2; Rare:34 | ||||
chr6:122399357-122399693 | Common:6; Rare:120 | ||||
chr6:122471773-122471937 | Common:3; Rare:49 | ||||
chr6:122779587-122779866 | Rare:64 | ||||
chr6:122789049-122789355 | Common:1; Rare:73 | ||||
chr6:124962875-124962985 | Rare:37 | ||||
chr6:124963157-124963384 | Common:1; Rare:67 | ||||
chr6:125749178-125749216 | Rare:4 | ||||
chr6:125749393-125749736 | Common:5; Rare:138 | ||||
chr6:125986435-125986552 | Rare:46 |