Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:125064217-125064284 | Rare:20 | ||||
chr3:126266515-126266791 | Common:2; Rare:57 | ||||
chr3:126275039-126275235 | Common:1; Rare:39 | ||||
chr3:126355937-126356232 | Rare:78 | ||||
chr3:128813105-128813481 | Rare:93; Clinvar:4 | ||||
chr3:130047015-130047179 | Common:2; Rare:12 | ||||
chr3:130111422-130111669 | Common:3; Rare:71 | ||||
chr3:131361588-131361923 | Common:3; Rare:101 | ||||
chr3:134462425-134462570 | Common:3; Rare:29 | ||||
chr3:134464056-134464325 | Common:1; Rare:49 | ||||
chr3:138601753-138601912 | Rare:24 | ||||
chr3:139352420-139352677 | Rare:52; Clinvar (benign):1 | ||||
chr3:141412940-141413099 | Common:1; Rare:25 | ||||
chr3:141881085-141881185 | Rare:20 | ||||
chr3:143654902-143655240 | Common:1; Rare:58 |