Additional file 2: Tables S1â S3. of Secondary structure impacts patterns of selection in human lncRNAs

Table S1. Chromosome, transcript start coordinates, transcript end coordinates, and transcript ID for each lncRNA of the functional set. Table S2. Chromosome, transcript start coordinates, transcript end coordinates, and transcript ID for each lncRNA of the broad set. Table S3. Mean number of SNPs in regions classified according to the presence or not of ESE motifs for the functional and broad human sets in the five major populations. (XLS 295 kb)

补充表S1：功能集中每条长链非编码RNA（lncRNA, long non-coding RNA）对应的染色体、转录起始坐标、转录终止坐标及转录本ID。
补充表S2：广谱集中每条长链非编码RNA对应的染色体、转录起始坐标、转录终止坐标及转录本ID。
补充表S3：统计了五大人群中，针对人类功能集与广谱集，按外显子剪接增强子（ESE motif, Exonic Splicing Enhancer）基序存在与否划分的区域内，单核苷酸多态性（SNP, Single Nucleotide Polymorphism）的平均数量。本数据集为XLS格式，文件大小295 KB。