Variant report

Variant	rs10082566
Chromosome Location	chr11:5328707-5328708
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:5327117..5329057-chr11:5524583..5527352,2	K562	blood:

Variant related genes	Relation type
ENSG00000213931	Chromatin interaction
ENSG00000167355	Chromatin interaction
ENSG00000196565	Chromatin interaction

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs11036815	0.92[CHB][hapmap];0.83[JPT][hapmap];0.89[ASN][1000 genomes]
rs11036849	1.00[CEU][hapmap];1.00[CHB][hapmap];0.82[JPT][hapmap];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12275342	0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12277703	0.92[CHB][hapmap];0.83[JPT][hapmap];0.89[ASN][1000 genomes]
rs12280760	0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12282313	0.89[ASN][1000 genomes]
rs12284766	1.00[CEU][hapmap];1.00[CHB][hapmap];0.83[JPT][hapmap];0.95[YRI][hapmap];0.92[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2723384	0.80[ASN][1000 genomes]
rs2736566	0.89[ASN][1000 genomes]
rs3886221	0.90[CHB][hapmap];0.89[ASN][1000 genomes]
rs3886222	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]
rs3886223	0.92[CHB][hapmap];0.82[JPT][hapmap];0.89[ASN][1000 genomes]
rs4578419	0.92[CHB][hapmap];0.83[JPT][hapmap];0.89[ASN][1000 genomes]
rs61227473	0.89[ASN][1000 genomes]
rs6578600	0.89[ASN][1000 genomes]
rs6578601	0.89[ASN][1000 genomes]
rs6578602	0.89[ASN][1000 genomes]
rs6578603	0.92[CHB][hapmap];0.83[JPT][hapmap];0.89[ASN][1000 genomes]
rs6578605	1.00[CEU][hapmap];1.00[CHB][hapmap];0.83[JPT][hapmap];0.87[TSI][hapmap];0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7115584	0.92[CHB][hapmap];0.86[ASN][1000 genomes]
rs7118086	0.92[CHB][hapmap];0.83[JPT][hapmap]
rs7118468	0.92[CHB][hapmap];0.83[JPT][hapmap];0.89[ASN][1000 genomes]
rs7128856	0.92[CHB][hapmap];0.83[JPT][hapmap];0.89[ASN][1000 genomes]
rs7129490	0.92[CHB][hapmap];0.83[JPT][hapmap];0.89[ASN][1000 genomes]
rs72873015	0.89[ASN][1000 genomes]
rs72873016	0.88[ASN][1000 genomes]
rs7925940	0.89[ASN][1000 genomes]
rs7932505	0.80[JPT][hapmap];0.92[ASN][1000 genomes]
rs7932632	0.91[CHB][hapmap];0.81[JPT][hapmap];0.89[ASN][1000 genomes]
rs7935554	0.92[CHB][hapmap];0.83[JPT][hapmap];0.89[ASN][1000 genomes]
rs7935560	0.92[CHB][hapmap];0.82[JPT][hapmap];0.89[ASN][1000 genomes]
rs7942925	1.00[CEU][hapmap];1.00[CHB][hapmap];0.83[JPT][hapmap];0.87[TSI][hapmap];0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7944760	0.89[ASN][1000 genomes]
rs7946240	0.91[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.83[JPT][hapmap];0.87[TSI][hapmap];0.95[YRI][hapmap];0.92[AFR][1000 genomes];0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7946350	0.92[CHB][hapmap];0.83[JPT][hapmap];0.92[ASN][1000 genomes]
rs7946616	0.92[CHB][hapmap];0.81[JPT][hapmap];0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1042613	chr11:5173410-5336839	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
2	nsv1052750	chr11:5187571-5338802	Enhancers Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
3	nsv1048355	chr11:5192334-5336839	Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
4	nsv1037760	chr11:5228195-5338802	Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
5	nsv1054068	chr11:5228264-5336839	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Strong transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
6	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
7	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

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:5325800-5330400	Strong transcription	K562	blood
2	chr11:5327200-5328800	Enhancers	NHDF-Ad	bronchial

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