Additional file 2 of Inversion polymorphism in a complete human genome assembly

Additional file 2: Table S1. Nonredundant inversion callset reported in this study. Table S2. Putative novel inversions with respect to T2T-CHM13 reference. Table S3. Enrichment of inversions in pericentromeric regions. Table S4. List of minor alleles and resolved orientation errors in GRCh38. Table S5. Novel inversions in HPRC Strand-seq dataset.附加文件2：表S1。本研究报道的非冗余倒位变异集。表S2。相较于T2T-CHM13参考基因组的推定新型倒位。表S3。着丝粒旁区倒位的富集特征。表S4。GRCh38参考基因组中的次要等位基因及已校正方向误差列表。表S5。HPRC链测序（Strand-seq）数据集中的新型倒位。