Table 1.

Variants within MYC-335 revealed by sequencing 727 control samples

				Minor allele frequency
Variation	Type	Location chr8	TF binding site	U.K.	Finland	YRI	SW AFAM	Korea
rs6983267a	G>T	128413305	TCF4	0.541	0.535	0.977	0.822	0.389
rs34835043	A>G	128413389		0.038	0.056	0.069	0.028	0.069
rs73706717	T>C	128413510		0	0	0.117	0.128	0
Novel 1	G>A	128413593		0	0	0.017	0.017	0
Novel 2	G>T	128413783		0.081	0.115	0	0.022	0
rs67180956	T>C	128413809	Broad Complex 3	0.041	0.057	0.138	0.094	0.069
Novel 3	G>A	128413829		0	0	0.003	0	0
rs7008058	T>C	128413978		0	0	0.117	0.128	0
Novel 4	G>A	128413985		0	0.003	0	0	0
Novel 5	C>T	128414065		0	0.003	0	0	0
rs67491583	Del GA	128414232e128414233	GFI1	0	0	0.089	0.056	0
Novel 6	C>T	128414371		0.067	0.075	0.028	0.017	0.028
Novel 7	G>C	128414372		0	0	0.006	0	0

^aFrequency of the risk allele G is presented.