Variant report

Variant	rs10896733
Chromosome Location	chr11:58036382-58036383
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 59 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:55)

rs_ID	r²[population]
rs10736689	0.85[AMR][1000 genomes]
rs10750890	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10750891	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10792156	1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.92[MEX][hapmap];1.00[TSI][hapmap];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10792157	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10792163	0.85[AMR][1000 genomes]
rs10792164	0.85[AMR][1000 genomes]
rs10792167	0.83[AMR][1000 genomes]
rs10896723	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10896740	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10896743	0.89[AMR][1000 genomes];0.80[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10896745	0.87[AMR][1000 genomes]
rs10896751	0.85[AMR][1000 genomes]
rs10896752	0.85[AMR][1000 genomes]
rs10896767	0.83[AMR][1000 genomes]
rs10896768	0.83[AMR][1000 genomes]
rs11229332	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11229334	0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11229337	0.82[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11229351	0.84[AMR][1000 genomes]
rs11229354	0.85[AMR][1000 genomes]
rs11229356	0.85[AMR][1000 genomes]
rs11229367	0.85[AMR][1000 genomes]
rs11229368	0.82[AMR][1000 genomes]
rs11229376	0.83[AMR][1000 genomes]
rs11603523	0.85[AMR][1000 genomes]
rs12794193	0.85[AMR][1000 genomes]
rs12806327	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1938648	0.83[AMR][1000 genomes]
rs1938661	0.85[AMR][1000 genomes]
rs2003230	0.83[AMR][1000 genomes]
rs2186408	0.83[AMR][1000 genomes]
rs2211942	0.85[AMR][1000 genomes]
rs4127350	0.85[AMR][1000 genomes]
rs4127351	0.83[AMR][1000 genomes]
rs4127352	0.85[AMR][1000 genomes]
rs4453250	0.85[AMR][1000 genomes]
rs4581466	0.85[CHB][hapmap];0.83[CHD][hapmap];0.90[JPT][hapmap]
rs4644660	0.82[AMR][1000 genomes]
rs4939192	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4939204	0.85[AMR][1000 genomes]
rs6591470	0.85[AMR][1000 genomes]
rs7105115	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7112250	0.83[AMR][1000 genomes]
rs7115653	0.85[AMR][1000 genomes]
rs7117845	0.84[CHB][hapmap];0.95[JPT][hapmap];0.90[YRI][hapmap];0.85[AMR][1000 genomes]
rs7129144	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs746248	0.83[AMR][1000 genomes]
rs7480112	0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7926438	0.92[AMR][1000 genomes];0.80[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7934850	0.87[AMR][1000 genomes]
rs7944257	0.95[JPT][hapmap];0.86[AMR][1000 genomes]
rs7944352	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7948107	0.85[AMR][1000 genomes]
rs947785	1.00[CEU][hapmap];0.90[CHB][hapmap];0.95[JPT][hapmap];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[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	nsv1054205	chr11:57544264-58358509	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
2	nsv897589	chr11:57623815-58052357	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
3	nsv1039453	chr11:57924680-58119650	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
4	nsv541051	chr11:57924680-58119650	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 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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