Variant report

Variant	rs10736677
Chromosome Location	chr11:56326343-56326344
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 94 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:86)

rs_ID	r²[population]
rs10400288	0.91[ASN][1000 genomes]
rs10501354	1.00[CHB][hapmap];0.88[CHD][hapmap];1.00[JPT][hapmap]
rs10736676	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap]
rs10736678	1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[YRI][hapmap]
rs10750820	1.00[CHB][hapmap];0.88[CHD][hapmap];0.90[JPT][hapmap];0.91[ASN][1000 genomes]
rs10792038	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.97[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap]
rs10792039	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap]
rs10792040	1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs10792043	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10896480	0.93[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs10896501	0.82[ASN][1000 genomes]
rs10896513	0.80[TSI][hapmap]
rs11228212	0.86[CHB][hapmap];0.90[JPT][hapmap];0.91[ASN][1000 genomes]
rs11228641	1.00[CHB][hapmap];0.94[CHD][hapmap];1.00[JPT][hapmap]
rs11228673	1.00[CHB][hapmap];0.90[JPT][hapmap]
rs11228676	0.94[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.88[LWK][hapmap];1.00[MEX][hapmap];0.91[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap]
rs11228684	0.91[ASN][1000 genomes]
rs11228686	0.91[ASN][1000 genomes]
rs11228687	1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs11228693	1.00[CHB][hapmap];0.94[CHD][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs11228694	0.85[ASN][1000 genomes]
rs11228698	0.85[ASN][1000 genomes]
rs11228701	0.85[ASN][1000 genomes]
rs11228706	1.00[CHB][hapmap];0.94[CHD][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs11228708	1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs11228710	0.88[ASW][hapmap]
rs11228759	0.88[CHD][hapmap];0.91[JPT][hapmap]
rs11228760	0.88[CHD][hapmap];0.91[JPT][hapmap]
rs11228763	0.88[CHD][hapmap];0.91[JPT][hapmap]
rs11228769	0.90[JPT][hapmap]
rs12222989	0.85[ASN][1000 genomes]
rs12223492	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12418150	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs12418301	0.91[ASN][1000 genomes]
rs1397048	0.80[TSI][hapmap]
rs1397050	0.91[MKK][hapmap]
rs1473592	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1605924	0.91[ASN][1000 genomes]
rs17150739	0.97[ASN][1000 genomes]
rs1945196	0.97[ASN][1000 genomes]
rs1945206	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1945210	1.00[CHB][hapmap];0.90[JPT][hapmap];0.91[ASN][1000 genomes]
rs1945261	1.00[CHB][hapmap];0.94[CHD][hapmap];1.00[JPT][hapmap]
rs1945263	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1945282	1.00[CHB][hapmap];0.94[CHD][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap]
rs2202932	0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2511143	1.00[YRI][hapmap];0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2865516	1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs33995115	1.00[CHB][hapmap];0.94[CHD][hapmap];1.00[JPT][hapmap]
rs3938998	1.00[CHB][hapmap];0.88[CHD][hapmap];0.90[JPT][hapmap];0.91[ASN][1000 genomes]
rs4382928	0.82[EUR][1000 genomes]
rs4500505	0.97[ASN][1000 genomes]
rs4939034	1.00[CHB][hapmap];0.90[JPT][hapmap]
rs4939043	0.91[ASN][1000 genomes]
rs4939061	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.93[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs4939065	0.94[ASW][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];1.00[JPT][hapmap];0.97[LWK][hapmap];0.87[MKK][hapmap];0.96[YRI][hapmap]
rs4939066	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap]
rs583216	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap]
rs583589	0.97[ASN][1000 genomes]
rs584608	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.93[ASN][1000 genomes]
rs588805	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs592744	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs596212	0.84[AFR][1000 genomes];0.93[AMR][1000 genomes];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs597680	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap]
rs600187	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap]
rs611397	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap]
rs614942	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs61710550	0.85[ASN][1000 genomes]
rs628524	0.88[ASW][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];1.00[JPT][hapmap];0.97[LWK][hapmap];0.86[MKK][hapmap];0.96[YRI][hapmap]
rs637912	0.97[ASN][1000 genomes]
rs642630	0.97[ASN][1000 genomes]
rs643384	0.97[ASN][1000 genomes]
rs645351	0.88[ASW][hapmap];1.00[CHB][hapmap];0.88[CHD][hapmap];1.00[JPT][hapmap];0.97[LWK][hapmap];0.87[MKK][hapmap];0.96[YRI][hapmap]
rs646286	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap]
rs654634	0.97[ASN][1000 genomes]
rs655779	0.81[AFR][1000 genomes];0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs656565	0.97[ASN][1000 genomes]
rs6591323	1.00[CHB][hapmap];0.88[CHD][hapmap];0.90[JPT][hapmap]
rs6591381	1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs674431	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs676901	0.97[ASN][1000 genomes]
rs688832	0.94[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.97[LWK][hapmap];1.00[MEX][hapmap];0.98[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap]
rs7924528	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap]
rs7928704	1.00[CHB][hapmap];0.88[CHD][hapmap];0.90[JPT][hapmap]
rs7939886	0.97[ASN][1000 genomes]
rs971758	1.00[CHB][hapmap];0.88[CHD][hapmap];0.81[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1050024	chr11:55900482-56518943	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	52 gene(s)	inside rSNPs	diseases
2	nsv497854	chr11:55917298-56537994	Enhancers ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	50 gene(s)	inside rSNPs	diseases
3	nsv971949	chr11:56126625-56344170	Enhancers Weak transcription ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region	18 gene(s)	inside rSNPs	diseases
4	nsv468576	chr11:56299930-56420029	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
5	nsv555099	chr11:56299930-56420029	Enhancers Active TSS Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
6	nsv516558	chr11:56315297-56347636	Weak transcription Enhancers	TF binding region CpG island	2 gene(s)	inside rSNPs	diseases
7	esv2421725	chr11:56323407-56354044	Enhancers Weak transcription	TF binding region CpG island	1 gene(s)	inside rSNPs	diseases
8	nsv523453	chr11:56324576-56366677	Enhancers Weak transcription	TF binding region CpG island	2 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs10736677	OR5B2	cis	parietal	SCAN
rs10736677	PUS3	trans	parietal	SCAN
rs10736677	MS4A3	cis	parietal	SCAN

Chromatin state (count:1 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:56326200-56326600	Enhancers	Rectal Mucosa Donor 29	rectum

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