Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:193593081-193593404 | Rare:100; Clinvar:2; Clinvar (benign):2 | ||||
chr3:194487020-194487146 | Common:3; Rare:61 | ||||
chr3:195543127-195543493 | Common:4; Rare:125 | ||||
chr3:195584097-195584405 | Common:12; Rare:62 | ||||
chr3:195895922-195895990 | Rare:28 | ||||
chr3:196082048-196082309 | Common:5; Rare:101 | ||||
chr3:196287658-196287831 | Common:1; Rare:52 | ||||
chr3:196318163-196318342 | Common:1; Rare:78 | ||||
chr3:196432385-196432494 | Common:1; Rare:50 | ||||
chr3:196503563-196503929 | Common:7; Rare:122 | ||||
chr3:196568518-196568619 | Common:1; Rare:25 | ||||
chr3:196639608-196639824 | Common:2; Rare:47 | ||||
chr3:196712171-196712358 | Common:3; Rare:62 | ||||
chr3:196867748-196867983 | Rare:85 | ||||
chr3:196942375-196942686 | Common:1; Rare:131 |