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Occurrences of woolly mammoth SNV combinations in reads for RNase L domain variants. Read counts for Wrangel, M4, Oimyakon, and M25 are left of reads. Read counts in parentheses indicate addition of inferred counts based on the observation that SNVs for residues 675 and 680 always co-occur. Most frequent haplotypes highlighted in gray. Residue number above reads. SNV combinations with no occurrences are not shown.
