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. 2014 Dec;24(12):2066–2076. doi: 10.1101/gr.180893.114

Figure 4.

Figure 4.

Functional consequences of CHM1 heterozygous variants not in repetitive sequence (HNR variants). Approximately 97% of HNR variants are intergenic or intronic. Of the remaining 3% of other variants, ∼48% are in the 3′ or 5′ UTR, 17% are silent, and 35% are coding (missense, nonsense, essential splice site).