Table 1. Association data for the most significant SNPs in the case-control study of all CUP patients shown in Figure 1.

SNP	Chr	Position	Risk allele*	MAFctrl	OR_het	OR_hom	P_Geno	OR_Allele	P_Allele	P**	I2**	Gene	Location	Distance
rs9347983	6	165386880	G	0.24	1.45	1.85	1.1×10−5	1.40	1.4×10−6	0.46	0.0	RP11-300M24.1	flanking 3′UTR	224kb
rs741828	7	155616377	T	0.25	1.46	2.06	7.2×10−7	1.44	1.1×10−7	0.19	40.0	Y RNA	flanking 3′UTR	55Kb
rs2660852	12	94969679	C	0.36	1.33	2.50	7.4×10−7	1.44	1.9×10−7	0.81	0.0	LTA4H	flanking 5′UTR	8.2kb
rs4771282	13	97144122	T	0.39	1.56	1.94	7.4×10−7	1.40	1.4×10−7	0.35	3.9	RP11-12OE13.1	flanking 5′UTR	16Kb
rs477145	21	31684281	T	0.31	1.47	1.93	1.2×10−6	1.42	1.1×10−7	0.05	66.9	TIAM1	intron	−50673
rs2835931	21	38043518	T	0.24	1.53	1.89	1.8×10−6	1.43	4.0×10−7	0.51	0.0	KCNJ6	intron	−34214

^*The risk is calculated to the risk allele

^**Heterogeneity for data from the 3 centers