Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:130111485-130111738 | Common:3; Rare:63 | ||||
chr3:130112386-130112556 | Common:2; Rare:50 | ||||
chr3:131361595-131361917 | Common:3; Rare:99 | ||||
chr3:139373385-139373692 | Rare:56 | ||||
chr3:143528945-143529178 | Rare:44 | ||||
chr3:152205408-152205565 | Common:1; Rare:18 | ||||
chr3:153164043-153164057 | Rare:3 | ||||
chr3:156527229-156527334 | Rare:18 | ||||
chr3:156816941-156817218 | Common:1; Rare:98 | ||||
chr3:157156784-157157066 | Rare:29 | ||||
chr3:157174861-157175163 | Common:3; Rare:130 | ||||
chr3:160515176-160515470 | Common:1; Rare:64 | ||||
chr3:169765058-169765274 | Rare:78; Clinvar (pathogenic):1 | ||||
chr3:172509319-172509421 | Common:1; Rare:19 | ||||
chr3:184710815-184710829 | Rare:2 |