Variant report

Variant	rs11986411
Chromosome Location	chr8:51654055-51654056
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 111 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:104)

rs_ID	r²[population]
rs10087228	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs10087953	0.95[ASN][1000 genomes]
rs10097209	1.00[ASN][1000 genomes]
rs10097404	1.00[ASN][1000 genomes]
rs10099033	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs10101076	0.94[ASN][1000 genomes]
rs10110050	0.85[ASN][1000 genomes]
rs10111045	0.90[CHB][hapmap];0.94[JPT][hapmap];0.87[ASN][1000 genomes]
rs1018207	1.00[CHB][hapmap];1.00[CHD][hapmap];0.85[GIH][hapmap];0.89[JPT][hapmap]
rs10216649	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs10429378	0.85[ASN][1000 genomes]
rs10958023	1.00[CHB][hapmap];0.89[JPT][hapmap];0.85[ASN][1000 genomes]
rs10958026	0.85[ASN][1000 genomes]
rs10958061	1.00[ASN][1000 genomes]
rs10958065	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10958066	0.96[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10958080	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10958115	0.84[CEU][hapmap];0.80[CHB][hapmap];0.92[CHD][hapmap];0.95[JPT][hapmap]
rs10958117	0.84[CEU][hapmap]
rs10958140	0.81[ASN][1000 genomes]
rs11775633	0.84[CEU][hapmap];0.80[CHB][hapmap];0.95[JPT][hapmap]
rs11785968	0.94[ASN][1000 genomes]
rs11997970	0.85[ASN][1000 genomes]
rs12542948	0.81[ASN][1000 genomes]
rs12681280	0.99[ASN][1000 genomes]
rs12681303	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13250468	0.87[ASN][1000 genomes]
rs13251712	0.81[ASN][1000 genomes]
rs13251980	0.84[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs13252863	0.92[CEU][hapmap]
rs13254513	0.87[CEU][hapmap];0.89[TSI][hapmap]
rs13258680	0.81[ASN][1000 genomes]
rs13261493	0.83[ASN][1000 genomes]
rs13263172	0.89[ASN][1000 genomes]
rs13269724	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs13271305	0.89[ASN][1000 genomes]
rs13277400	0.81[ASN][1000 genomes]
rs1396377	1.00[CHB][hapmap];0.97[CHD][hapmap];0.84[GIH][hapmap];0.89[JPT][hapmap];0.85[ASN][1000 genomes]
rs1472907	0.85[ASN][1000 genomes]
rs1483642	0.87[CEU][hapmap]
rs1508621	0.84[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs1508622	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1508623	0.92[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap];0.81[ASN][1000 genomes]
rs1567311	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.85[GIH][hapmap];1.00[JPT][hapmap];0.92[TSI][hapmap];0.81[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs16915417	0.83[ASN][1000 genomes]
rs1911830	0.92[CEU][hapmap];0.89[TSI][hapmap]
rs1911835	0.99[ASN][1000 genomes]
rs1911836	0.82[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap]
rs2170856	0.83[ASN][1000 genomes]
rs2170857	0.83[ASN][1000 genomes]
rs2202797	0.84[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap];0.85[ASN][1000 genomes]
rs2392761	0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28470779	0.98[ASN][1000 genomes]
rs28647321	0.98[ASN][1000 genomes]
rs28683156	0.89[ASN][1000 genomes]
rs28815525	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34486025	1.00[ASN][1000 genomes]
rs34871864	1.00[CHB][hapmap];1.00[CHD][hapmap];0.83[GIH][hapmap];0.89[JPT][hapmap];0.85[ASN][1000 genomes]
rs35521388	1.00[ASN][1000 genomes]
rs3999808	1.00[ASN][1000 genomes]
rs4242462	1.00[CHB][hapmap];0.89[JPT][hapmap];0.81[ASN][1000 genomes]
rs4382493	0.83[ASN][1000 genomes]
rs4422788	0.84[CEU][hapmap];0.80[CHB][hapmap];0.92[CHD][hapmap];0.95[JPT][hapmap];0.83[ASN][1000 genomes]
rs4873153	0.85[ASN][1000 genomes]
rs4873155	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs4873479	0.81[ASN][1000 genomes]
rs6473292	0.93[ASN][1000 genomes]
rs6473319	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs6473337	0.89[CHD][hapmap];0.84[JPT][hapmap]
rs66730072	1.00[ASN][1000 genomes]
rs67729017	0.89[ASN][1000 genomes]
rs6981207	0.83[ASN][1000 genomes]
rs6981429	0.83[ASN][1000 genomes]
rs6985321	0.83[ASN][1000 genomes]
rs6987633	0.85[ASN][1000 genomes]
rs6988562	0.84[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6988854	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6991518	0.91[ASN][1000 genomes]
rs6992341	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs6992551	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];1.00[ASN][1000 genomes]
rs6999211	0.85[ASN][1000 genomes]
rs7002119	0.91[ASN][1000 genomes]
rs7009895	0.97[ASN][1000 genomes]
rs7011647	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7012338	0.93[ASN][1000 genomes]
rs7013183	0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7013366	1.00[CHB][hapmap];0.89[JPT][hapmap];0.85[ASN][1000 genomes]
rs7015370	0.83[ASN][1000 genomes]
rs7018197	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs7460470	1.00[ASN][1000 genomes]
rs7812344	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs7816024	0.95[CHB][hapmap];1.00[JPT][hapmap]
rs7820724	0.83[ASN][1000 genomes]
rs7822224	0.95[CHB][hapmap];0.97[CHD][hapmap];0.83[GIH][hapmap];0.94[JPT][hapmap];0.99[ASN][1000 genomes]
rs7829079	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7831651	0.84[CEU][hapmap]
rs7833823	0.83[ASN][1000 genomes]
rs7834256	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7834585	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs7844393	1.00[CHB][hapmap];0.94[JPT][hapmap];0.83[ASN][1000 genomes]
rs7845831	1.00[ASN][1000 genomes]
rs7846699	0.84[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.85[GIH][hapmap];1.00[JPT][hapmap]
rs906656	0.92[CEU][hapmap];0.92[TSI][hapmap]
rs936722	0.81[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	nsv948436	chr8:51115028-51917504	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv531502	chr8:51390997-51703556	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	esv3514165	chr8:51416583-51923545	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	esv3514166	chr8:51416583-51923545	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv1027452	chr8:51525439-51725489	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv1019760	chr8:51628619-51862150	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	nsv1029698	chr8:51628619-51863635	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	2 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
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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