Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:189010001-189010365 | Common:1; Rare:78; Clinvar:6; Clinvar (benign):7; Clinvar (pathogenic):3 | ||||
chr2:189049353-189049737 | Common:5; Rare:76; Clinvar:5; Clinvar (benign):1 | ||||
chr2:189286372-189286593 | Common:3; Rare:28 | ||||
chr2:193171145-193171237 | Common:1; Rare:35 | ||||
chr2:193502627-193502802 | Common:5; Rare:61 | ||||
chr2:195614007-195614183 | Rare:28 | ||||
chr2:196233029-196233249 | Common:3; Rare:49 | ||||
chr2:196259990-196260034 | Rare:7 | ||||
chr2:196260060-196260239 | Common:1; Rare:36 | ||||
chr2:205712482-205712744 | Common:2; Rare:27 | ||||
chr2:207334600-207334800 | Common:1; Rare:32 | ||||
chr2:207394768-207394997 | Common:3; Rare:42 | ||||
chr2:215433563-215433833 | Common:1; Rare:57 | ||||
chr2:215717954-215718212 | Common:1; Rare:43 | ||||
chr2:216316057-216316301 | Common:2; Rare:53 |