Variant report

Variant	rs11593951
Chromosome Location	chr10:56043784-56043785
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 58 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs1020198	1.00[JPT][hapmap]
rs1020199	1.00[JPT][hapmap]
rs1020200	1.00[JPT][hapmap]
rs10763101	0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10825267	1.00[JPT][hapmap]
rs10825269	1.00[JPT][hapmap]
rs10825270	1.00[JPT][hapmap]
rs10825313	1.00[YRI][hapmap]
rs11004129	1.00[JPT][hapmap]
rs11004201	1.00[JPT][hapmap];1.00[YRI][hapmap]
rs11004211	0.99[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11004212	0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11004214	0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11004222	0.95[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs11004225	0.95[CEU][hapmap];1.00[JPT][hapmap]
rs11004233	0.95[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs11004249	1.00[YRI][hapmap]
rs11004251	1.00[YRI][hapmap]
rs11816146	1.00[JPT][hapmap]
rs11816562	1.00[JPT][hapmap]
rs12242300	1.00[JPT][hapmap]
rs12356885	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12357807	0.90[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs12358760	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12358864	0.94[CEU][hapmap];1.00[YRI][hapmap]
rs12762518	0.91[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs12764585	1.00[YRI][hapmap]
rs12768441	0.95[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs12770667	0.95[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs12775251	0.99[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12780283	0.95[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs16905671	1.00[JPT][hapmap]
rs16905674	1.00[JPT][hapmap]
rs16905760	1.00[JPT][hapmap]
rs2044000	1.00[JPT][hapmap]
rs2096174	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4295959	1.00[JPT][hapmap]
rs4313480	1.00[JPT][hapmap]
rs7084434	1.00[JPT][hapmap]
rs7087966	1.00[JPT][hapmap]
rs7095082	1.00[JPT][hapmap]
rs7893192	1.00[JPT][hapmap]
rs7893350	1.00[JPT][hapmap]
rs7898758	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7901367	0.95[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7901520	1.00[JPT][hapmap]
rs7916480	1.00[JPT][hapmap]
rs7921598	1.00[JPT][hapmap]
rs978841	0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv948730	chr10:55845301-56093271	ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
2	nsv1054364	chr10:55925471-56196447	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv540633	chr10:55925471-56196447	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	esv20105	chr10:55939729-56047721	ZNF genes & repeats Enhancers Weak transcription Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv1053832	chr10:56022197-56061600	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
6	esv2753511	chr10:56022197-56153636	Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	nsv6698	chr10:56030123-56074572	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
8	nsv1044020	chr10:56038546-56224736	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
9	nsv540634	chr10:56038546-56224736	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region	2 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	chr10:56043600-56044000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived

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