Variant report

Variant	rs11228697
Chromosome Location	chr11:56414871-56414872
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	E2F4	chr11:56414821-56414943	MCF10A-Er-Src	breast:	n/a	n/a

Variant related genes	Relation type
OR5AP2	TF binding region

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10896484	0.91[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs10896486	0.91[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs10896488	0.91[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs10896494	0.90[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs10896495	0.91[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs10896498	0.81[ASN][1000 genomes]
rs11228647	0.91[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs11228675	0.84[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs11228685	0.91[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs11228704	0.90[ASN][1000 genomes]
rs11228705	0.90[ASN][1000 genomes]
rs11228717	0.91[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs11228729	0.80[ASN][1000 genomes]
rs12225008	0.91[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs12365813	0.91[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs1397054	0.82[CHB][hapmap];0.93[JPT][hapmap];1.00[YRI][hapmap];0.90[ASN][1000 genomes]
rs1510004	0.91[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs4938829	0.84[JPT][hapmap];1.00[YRI][hapmap]
rs4938835	0.91[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.85[ASN][1000 genomes]
rs605734	1.00[YRI][hapmap]
rs611459	0.91[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs624412	0.81[CHB][hapmap];1.00[YRI][hapmap]
rs640953	1.00[JPT][hapmap]
rs652537	0.84[CEU][hapmap];1.00[YRI][hapmap]
rs675991	1.00[YRI][hapmap]
rs72915700	0.93[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	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	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
4	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
5	nsv971952	chr11:56361311-56452186	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
6	nsv949349	chr11:56371633-56593610	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	18 gene(s)	inside rSNPs	diseases
7	nsv1051853	chr11:56393347-56523720	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
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