Abstract
Abstract Blood samples were collected from unrelated individuals of the Chinese Han ethnic group in Chengdu, China. DNA was extracted using the Chelex method (1). PCR amplification conditions can be accessed at http://www.legalmed.org/dna/DXS6804.htm. The volume of PCR reaction for each locus was 37.5 µL. The PCR products were analyzed by horizontal nondenaturing polyacrylamide gel electrophoresis with a discontinuous buffer system and visualized by silver staining (2). Data of female population genetics and forensic science were analyzed using the POWERSTATS program (3). The complete dataset can be accessed at http://www.legalmed. org/dna/DXS6804.htm
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