Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:15795035-15795229 | Common:1; Rare:46 | ||||
chr3:31226395-31226711 | Common:3; Rare:56 | ||||
chr3:40453142-40453484 | Common:7; Rare:81 | ||||
chr3:41229946-41230228 | Rare:49 | ||||
chr3:47418625-47418682 | Common:1; Rare:18 | ||||
chr3:49357211-49357300 | Rare:20 | ||||
chr3:71755318-71755741 | Rare:77 | ||||
chr3:75435094-75435345 | Common:2; Rare:87 | ||||
chr3:81761530-81761556 | Common:4; Rare:3; Clinvar (benign):1 | ||||
chr3:87089151-87089310 | Common:2; Rare:30 | ||||
chr3:87792605-87793224 | Common:6; Rare:162 | ||||
chr3:87793448-87793659 | Rare:29 | ||||
chr3:101676284-101676478 | Rare:62 | ||||
chr3:107240512-107240749 | Rare:90 | ||||
chr3:119323015-119323291 | Common:1; Rare:57 |