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Supplementary Table 1. Resequencing results.
ID/position Variation Location Frequency (sample)
Frequency (dbSNP) rs11664064 SNP A/G Intron 7 11% 2%
rs45612637 SNP G/A Intron 5 3.0% 4.2%
12,875,055 TTAAGT- Promoter <0.1% New 12,875,251 SNP T/A Promoter 5% New rs35923716 SNP T/C Promoter 33.7% 11.1%
rs45524731 CT- Promoter 4.2% NA
rs45564442 TTCAT- Promoter 2.1% NA rs45576131 SNP G/C Promoter 4.3% 97%
rs35954636 SNP A/C Promoter 33.3% 11.1%
Identity of the variation is indicated by the NCBI (http://wwwncbinlmnihgov) rs ID and if new by the base position position according to Ensembl database (http://wwwensemblorg) NA=not available dbSNP frequencies were acquired from the NCBI dbSNP database.
