Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:81761642-81761657 | Rare:6 | ||||
chr3:101576984-101577253 | Common:2; Rare:65 | ||||
chr3:101680985-101681156 | Common:2; Rare:37 | ||||
chr3:107240650-107240718 | Rare:28 | ||||
chr3:110969832-110970150 | Rare:60 | ||||
chr3:120095037-120095276 | Common:1; Rare:71 | ||||
chr3:130112400-130112547 | Common:2; Rare:37 | ||||
chr3:147940002-147940037 | Rare:7 | ||||
chr3:157174883-157175253 | Common:3; Rare:161 | ||||
chr3:159732222-159732390 | Common:1; Rare:34 | ||||
chr3:168249535-168249685 | Common:1; Rare:39 | ||||
chr3:169765043-169765207 | Rare:73; Clinvar:2; Clinvar (pathogenic):2 | ||||
chr3:181174967-181175097 | Common:1; Rare:19 | ||||
chr3:181699644-181699778 | Common:1; Rare:26 | ||||
chr3:181710505-181710709 | Rare:42 |