Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:152269533-152269689 | Rare:41 | ||||
chr3:155854371-155854774 | Rare:113 | ||||
chr3:155870323-155870732 | Common:2; Rare:118 | ||||
chr3:156674370-156674664 | Common:3; Rare:84 | ||||
chr3:157160042-157160343 | Rare:123 | ||||
chr3:157436826-157436885 | Rare:14 | ||||
chr3:157543223-157543400 | Rare:42 | ||||
chr3:158105732-158105893 | Common:5; Rare:80; Clinvar:1; Clinvar (benign):1 | ||||
chr3:158801802-158802168 | Common:3; Rare:127 | ||||
chr3:160399175-160399288 | Rare:27; Clinvar:2 | ||||
chr3:160399518-160399669 | Rare:31 | ||||
chr3:161221209-161221360 | Common:2; Rare:50 | ||||
chr3:169773331-169773427 | Rare:30 | ||||
chr3:170908562-170908837 | Common:1; Rare:76 | ||||
chr3:172711048-172711208 | Rare:62 |