“…All the allelic frequency data of 30 InDel markers from 100 populations, including African, (Northern and Southern) American, European, and Asian, were collected as the dataset f. Since the genotype data could not be found in some populations in their reports, we sorted out the genotype data from 52 populations as the dataset g, including an African, 3 European, 7 American, 41 Asian populations, and Guizhou Sui (Fondevila et al, 2012;Friis et al, 2012;Kis et al, 2012;Larue et al, 2012;Akhteruzzaman et al, 2013;Carvalho and Pinheiro, 2013;da silva et al, 2013;Martin et al, 2013;Kim et al, 2014;Ferreira Palha et al, 2015;Hefke et al, 2015;Meng et al, 2015;Guo et al, 2016Guo et al, , 2018Martinez-Cortes et al, 2016;Mei et al, 2016;Du et al, 2017Du et al, , 2019Kong et al, 2017;Li et al, 2018Li et al, , 2019Ma et al, 2018;Chen et al, 2019;He et al, 2019a,c;Jian et al, 2019;Liu Y. et al, 2020). The genome-wide SNP data of the Sui population were merged with the reference dataset including 1240 k, Human Origin, and so on (Patterson et al, 2012;Lipson et al, 2018;Mccoll et al, 2018;Liu D. et al, 2020;Ning et al, 2020;Yang et al, 2020;Wang C. C. et al, 2021) to generate two combined datasets covering 189,177 and 71,989 SNPs for subsequent analyses.…”