Variant report

Variant	rs3886222
Chromosome Location	chr11:5343995-5343996
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs10082566	0.90[CEU][hapmap];1.00[CHB][hapmap];0.87[TSI][hapmap];0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11036815	0.92[CHB][hapmap];1.00[CHD][hapmap];0.94[JPT][hapmap];0.93[LWK][hapmap];0.96[YRI][hapmap];0.88[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs11036849	0.86[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12275342	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12277703	0.92[CHB][hapmap];0.94[JPT][hapmap];0.98[ASN][1000 genomes]
rs12280760	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12282313	0.98[ASN][1000 genomes]
rs12284766	0.90[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2723384	0.88[ASN][1000 genomes]
rs2736566	0.98[ASN][1000 genomes]
rs3886221	0.90[CHB][hapmap];0.87[JPT][hapmap];0.99[ASN][1000 genomes]
rs3886223	0.92[CHB][hapmap];0.94[JPT][hapmap];0.99[ASN][1000 genomes]
rs4578419	0.92[CHB][hapmap];0.94[JPT][hapmap];0.99[ASN][1000 genomes]
rs60376796	0.84[ASN][1000 genomes]
rs60695036	0.86[ASN][1000 genomes]
rs61227473	0.98[ASN][1000 genomes]
rs6578600	0.98[ASN][1000 genomes]
rs6578601	0.98[ASN][1000 genomes]
rs6578602	0.99[ASN][1000 genomes]
rs6578603	0.92[CHB][hapmap];1.00[CHD][hapmap];0.94[JPT][hapmap];0.99[ASN][1000 genomes]
rs6578605	1.00[ASW][hapmap];0.90[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];0.94[JPT][hapmap];0.95[LWK][hapmap];1.00[MEX][hapmap];0.96[MKK][hapmap];1.00[TSI][hapmap];0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7115584	0.92[CHB][hapmap];0.88[JPT][hapmap];0.97[ASN][1000 genomes]
rs7118086	0.92[CHB][hapmap];1.00[CHD][hapmap];0.94[JPT][hapmap]
rs7118468	0.92[CHB][hapmap];0.97[CHD][hapmap];0.94[JPT][hapmap];0.98[ASN][1000 genomes]
rs7128856	0.92[CHB][hapmap];1.00[CHD][hapmap];0.94[JPT][hapmap];0.98[ASN][1000 genomes]
rs7129490	0.92[CHB][hapmap];1.00[CHD][hapmap];0.94[JPT][hapmap];0.98[ASN][1000 genomes]
rs72873015	0.98[ASN][1000 genomes]
rs72873016	0.96[ASN][1000 genomes]
rs7925940	0.98[ASN][1000 genomes]
rs7932505	0.93[JPT][hapmap];0.96[ASN][1000 genomes]
rs7932632	0.91[CHB][hapmap];0.93[JPT][hapmap];0.98[ASN][1000 genomes]
rs7935554	0.92[CHB][hapmap];1.00[CHD][hapmap];0.94[JPT][hapmap];0.98[ASN][1000 genomes]
rs7935560	0.92[CHB][hapmap];0.93[JPT][hapmap];0.98[ASN][1000 genomes]
rs7942925	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.94[JPT][hapmap];1.00[TSI][hapmap];0.80[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7944760	0.98[ASN][1000 genomes]
rs7946240	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.94[JPT][hapmap];0.88[MEX][hapmap];1.00[TSI][hapmap];0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7946350	0.92[CHB][hapmap];0.94[JPT][hapmap];0.96[ASN][1000 genomes]
rs7946616	0.92[CHB][hapmap];0.93[JPT][hapmap];0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv524400	chr11:5328361-5416622	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
2	nsv1048608	chr11:5328516-5645179	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	60 gene(s)	inside rSNPs	diseases
3	nsv1046068	chr11:5335943-6063742	Strong transcription Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Enhancers Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	89 gene(s)	inside rSNPs	diseases
4	nsv819271	chr11:5343554-5344613	Weak transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:5330400-5345000	Weak transcription	K562	blood

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