MOESM4 of Concurrent genome and epigenome editing by CRISPR-mediated sequence replacement

Additional file 4: Table S1. Counts of reads including both inverted and forward-oriented sequences that exactly matched the promoter, exon 1, splice donor, PAM mutations, and one of the three sets of allele-defining SNVs (wild-type, methylated or unmethylated) as well as unmatched sequences.

附加文件4：表S1。测序读段计数统计，涵盖两类序列的对应读段数量：一类为同时具备反向或正向取向，且与启动子、外显子1、剪接供体位点、PAM（Protospacer Adjacent Motif）突变位点完全匹配，并匹配三类等位基因特异性单核苷酸变异（Single Nucleotide Variant，SNV）中任意一类（野生型、甲基化型或非甲基化型）的序列；另一类为未匹配序列。