Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:201118457-201118733 | Rare:49 | ||||
chr2:201118744-201118884 | Rare:12 | ||||
chr2:201129282-201129574 | Rare:59 | ||||
chr2:201132617-201132960 | Rare:53 | ||||
chr2:201451441-201451838 | Common:2; Rare:102 | ||||
chr2:201642622-201642764 | Common:1; Rare:69; Clinvar (benign):1 | ||||
chr2:201780890-201780993 | Common:2; Rare:30; Clinvar:1; Clinvar (benign):2 | ||||
chr2:202238498-202238650 | Rare:52 | ||||
chr2:202265631-202265814 | Rare:69 | ||||
chr2:202911881-202912024 | Rare:30 | ||||
chr2:202912127-202912303 | Common:2; Rare:58 | ||||
chr2:203238662-203239040 | Common:1; Rare:110 | ||||
chr2:203239212-203239322 | Rare:34 | ||||
chr2:203328012-203328437 | Common:2; Rare:150 | ||||
chr2:203535246-203535549 | Common:3; Rare:132 |