Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:101682836-101683014 | Rare:33 | ||||
chr3:107240636-107240749 | Rare:50 | ||||
chr3:136987134-136987222 | Common:1; Rare:20 | ||||
chr3:144379543-144379646 | Common:1; Rare:16 | ||||
chr3:150323415-150323592 | Common:1; Rare:45 | ||||
chr3:150408860-150409198 | Rare:84 | ||||
chr3:161242295-161242535 | Common:1; Rare:50 | ||||
chr3:161282621-161282746 | Common:1; Rare:20 | ||||
chr3:169765058-169765315 | Rare:87; Clinvar (pathogenic):2 | ||||
chr3:187742392-187742705 | Common:1; Rare:52 | ||||
chr3:187743107-187743348 | Rare:56 | ||||
chr3:187744409-187744477 | Rare:24 | ||||
chr3:187773703-187773902 | Common:1; Rare:36 | ||||
chr3:189490571-189491024 | Common:8; Rare:90 | ||||
chr3:190321211-190321355 | Common:1; Rare:28 |