Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:143188721-143188754 | Rare:7 | ||||
chr4:151100810-151101006 | Rare:45 | ||||
chr4:151659891-151660012 | Common:2; Rare:18 | ||||
chr4:168924139-168924420 | Rare:68; Clinvar:4; Clinvar (benign):1 | ||||
chr4:176221153-176221473 | Common:3; Rare:104 | ||||
chr4:184813507-184813723 | Common:2; Rare:41 | ||||
chr4:184814173-184814191 | Rare:3 | ||||
chr4:184814204-184814467 | Common:3; Rare:41 | ||||
chr4:184815058-184815346 | Common:3; Rare:65 | ||||
chr4:185589071-185589140 | Rare:9 | ||||
chr5:194422-194565 | Rare:28 | ||||
chr5:1633922-1634060 | Common:2; Rare:47 | ||||
chr5:1883316-1883429 | Common:1; Rare:25 | ||||
chr5:8457590-8457765 | Common:2; Rare:53 | ||||
chr5:33461712-33461965 | Common:2; Rare:62 |