TABLE 2

Primers used for amplification of the nine exons of the CYP2C9 gene (PCR I) and for sequencing The location of each primer is given in accordance with LokusLink Version NT_030059.8 GI:27498938.

Primer Name	Primer Position	Primer Sequence (5′ to 3′)
E1F	37,832-37,853	CCAACCAAGTACAGTGAAACTG
E1R^a	38,491-38,509	TGAAGAAGGAACACAGCT
E2 + 3F	40,997-41,021	CCTGCTGAATATGTTGATGTGAGTA
E2 + 3R^a	41,830-41,849	AGCTAACAACCAGGACTCAT
E4F^b	46,861-46,879	TGTGATTCCCTCTGAAACA
E5F	48,259-48,280	GGAGGTCTGAGTCTAGGAAATG
E5R^a	48,771-48,790	TGCTTCTCAAGCATTACTGA
E6F^b	71,243-71,262	GCTGTGTGACTCAGCTAGCT
E6R^a,^b	71,955-71,974	AGTAGCTGGGATTACAGCCA
E7F	80,404-80,424	CATTTGTGCATCTGTAACCA
E7R^a	80,931-80,950	ACAGGTCCTAGTGTCTGGCA
E8F	85,217-85,236	TTGCAGGGCACTTTAGCAAG
E8R^a	85,747-85,768	TGGATTAACTCCCCAAAGTCCA
E9F	88,056-88,074	ATCCATCCACTCATCCATC
E9R^a	88,576-88,594	GAAACATAGGAAACTCTCCG

↵a Reverse primers
↵ b Elongase Enzyme Mix (Invitrogen) was used