Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:201116274-201116429 | Rare:29 | ||||
chr2:201117406-201117586 | Rare:20 | ||||
chr2:201118570-201118837 | Rare:43 | ||||
chr2:201183019-201183183 | Common:1; Rare:23; Clinvar (benign):2 | ||||
chr2:201258138-201258211 | Rare:16 | ||||
chr2:201260395-201260567 | Common:1; Rare:38 | ||||
chr2:201451345-201451826 | Common:2; Rare:123 | ||||
chr2:201642637-201642770 | Rare:68 | ||||
chr2:201643396-201643553 | Common:1; Rare:50; Clinvar:4; Clinvar (benign):2 | ||||
chr2:201780890-201781243 | Common:3; Rare:108; Clinvar:3; Clinvar (benign):2 | ||||
chr2:202238443-202238698 | Common:1; Rare:88; Clinvar:1 | ||||
chr2:202265655-202265785 | Rare:46 | ||||
chr2:202634817-202635009 | Common:4; Rare:73 | ||||
chr2:202911586-202911990 | Common:1; Rare:88 | ||||
chr2:202912128-202912298 | Common:2; Rare:57 |