Rsid	Chr	Position	P value	Ref	Alt	Gwas trait	Gene symbol	Variant type	PMID
rs3130933	chr6	31132085	0.000000016	T	C	Type 1 diabetes	POU5F1	nearGene-3	17632545
rs3130933	chr6	31132085	0.0000127	T	C	Rheumatoid arthritis	POU5F1	nearGene-3	17804836
rs3130933	chr6	31132085	0.000000321	T	C	Multiple sclerosis	POU5F1	nearGene-3	20598377
rs2394882	chr6	31132649	0.0000027	A	C	HIV-1 control	POU5F1	intron	21051598
rs2394882	chr6	31132649	0.00018	A	C	Self-reported allergy	POU5F1	intron	23817569
rs2106074	chr6	31133509	0.0000000000781	G	A	Multiple complex diseases	POU5F1	intron	17554300
rs2106074	chr6	31133509	0.00000133	G	A	Multiple sclerosis	POU5F1	intron	17660530
rs2106074	chr6	31133509	0.0000013	G	A	HIV-1 control	POU5F1	intron	21051598
rs2106074	chr6	31133509	0.00019	G	A	Self-reported allergy	POU5F1	intron	23817569
rs9501063	chr6	31133894	0.000015	G	C	Multiple complex diseases	POU5F1	UTR-5	17554300
rs9501063	chr6	31133894	0.0000229	G	C	Behcet's disease	POU5F1	UTR-5	pha002888
rs3130932	chr6	31133943	0.0000219	C	A	Orofacial clefts	POU5F1	UTR-5	20023658
rs3130932	chr6	31133943	0.000003	C	A	HIV-1 control	POU5F1	UTR-5	21051598
rs3130932	chr6	31133943	0.000099	C	A	Crohn's disease	POU5F1	UTR-5	23266558
rs3130932	chr6	31133943	0.000198	C	A	Self-reported allergy	POU5F1	UTR-5	23817569
rs9263800	chr6	31134599	0.000812	G	A	Multiple complex diseases	POU5F1	UTR-5	17554300
rs9263800	chr6	31134599	0.0000655	G	A	Behcet's disease	POU5F1	UTR-5	pha002888
rs3130931	chr6	31134888	0.000343	T	C	Crohn's disease	POU5F1	intron	23266558
rs3130931	chr6	31134888	0.0000114	T	C	Behcet's disease	POU5F1	intron	pha002888
rs9263804	chr6	31135706	0.00000265	C	T	Multiple complex diseases	POU5F1	intron	17554300
rs9263804	chr6	31135706	0.0000000000748	C	T	Multiple sclerosis	POU5F1	intron	17660530
rs9263804	chr6	31135706	0.0000096	C	T	Urinary metabolites	POU5F1	intron	21572414
rs200484944	chr6	31135735	0.0000297	A	AC	Behcet's disease	POU5F1	intron	pha002888
rs9263805	chr6	31135735	0.0000297	A	C	Behcet's disease	POU5F1	intron	pha002888
rs3130501	chr6	31136453	0.00000211	A	G	Multiple complex diseases	POU5F1	intron	17554300
rs3130501	chr6	31136453	0.000000000213	A	G	Multiple sclerosis	POU5F1	intron	17660530
rs3130501	chr6	31136453	0.0000229	A	G	Orofacial clefts	POU5F1	intron	20023658
rs3130501	chr6	31136453	0.0000096	A	G	Urinary metabolites	POU5F1	intron	21572414
rs3130501	chr6	31136453	0.00000002	A	G	Stevens-Johnson syndrome and toxic epidermal necrolysis (SJS-TEN)	POU5F1	intron	21801394
rs3130501	chr6	31136453	0.000222	A	G	Crohn's disease	POU5F1	intron	23266558
rs3130501	chr6	31136453	0.000006	A	G	Multiple myeloma	POU5F1	intron	23955597
rs3130501	chr6	31136453	0.0000000042	A	G	Type 2 diabetes	POU5F1	intron	24509480
rs3130502	chr6	31136666	0.000002	A	G	Multiple myeloma	POU5F1	intron	23955597
rs3132524	chr6	31136714	0.00000266	T	C	Multiple complex diseases	POU5F1	intron	17554300
rs3132524	chr6	31136714	0.0000000000905	T	C	Multiple sclerosis	POU5F1	intron	17660530
rs3132524	chr6	31136714	0.0000096	T	C	Urinary metabolites	POU5F1	intron	21572414
rs3132524	chr6	31136714	0.000000004	T	C	Type 2 diabetes	POU5F1	intron	24509480
rs3132523	chr6	31136832	0.000001	T	C	Multiple myeloma	POU5F1	intron	23955597
rs879882	chr6	31139452	0.0000002	T	C	Height	POU5F1	nearGene-5	20881960
rs879882	chr6	31139452	0.0000005	T	C	Multiple myeloma	POU5F1	nearGene-5	23955597
rs1265159	chr6	31140047	0.00000124	G	A	HIV-1 control	POU5F1	nearGene-5	20041166
rs1265159	chr6	31140047	0.00000000715	G	A	Vitiligo	POU5F1	nearGene-5	20526339
rs1265159	chr6	31140047	1.4e-57	G	A	Myasthenia gravis	POU5F1	nearGene-5	23055271
rs1265159	chr6	31140047	0.000017	G	A	Type 2 diabetes	POU5F1	nearGene-5	23209189
rs1265159	chr6	31140047	0.0000095	G	A	Systemic lupus erythematosus	POU5F1	nearGene-5	24871463