Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:186567281-186567475 | Common:3; Rare:50 | ||||
chr3:186783281-186783639 | Common:1; Rare:161 | ||||
chr3:186784120-186784477 | Common:1; Rare:143 | ||||
chr3:186806411-186806541 | Rare:41 | ||||
chr3:187139479-187139558 | Rare:25 | ||||
chr3:187737971-187738145 | Common:1; Rare:27 | ||||
chr3:187744939-187745139 | Rare:88 | ||||
chr3:188152902-188153041 | Common:1; Rare:22 | ||||
chr3:188153751-188154232 | Common:1; Rare:116 | ||||
chr3:189100059-189100173 | Common:1; Rare:14 | ||||
chr3:190322378-190322566 | Common:2; Rare:50 | ||||
chr3:190513903-190514140 | Common:2; Rare:64 | ||||
chr3:190862653-190862751 | Rare:23 | ||||
chr3:191329325-191329826 | Common:4; Rare:155; Clinvar (benign):1 | ||||
chr3:192917836-192918003 | Common:2; Rare:76 |