Variant report

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs10062554	1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10520950	1.00[CHB][hapmap];0.87[CHD][hapmap];0.82[JPT][hapmap]
rs10520951	1.00[CHB][hapmap];0.89[JPT][hapmap]
rs12651967	0.84[ASN][1000 genomes]
rs12654016	0.82[ASN][1000 genomes]
rs12656237	0.84[ASN][1000 genomes]
rs12657245	0.82[ASN][1000 genomes]
rs12657687	0.90[ASN][1000 genomes]
rs12658382	0.84[ASN][1000 genomes]
rs12659873	1.00[CHB][hapmap];0.91[JPT][hapmap];0.90[ASN][1000 genomes]
rs16899404	1.00[CHB][hapmap];0.83[JPT][hapmap]
rs57047163	1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs57353106	0.82[ASN][1000 genomes]
rs73077041	0.82[ASN][1000 genomes]
rs73077048	0.82[ASN][1000 genomes]
rs73077049	0.82[ASN][1000 genomes]
rs73077055	0.82[ASN][1000 genomes]
rs73077059	0.87[ASN][1000 genomes]
rs73077061	0.84[ASN][1000 genomes]
rs73077062	0.87[ASN][1000 genomes]
rs7732091	1.00[MEX][hapmap]

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	esv3385368	chr5:29548608-29910057	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv1018779	chr5:29861138-29937229	Enhancers Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv1029641	chr5:29861138-29940871	Enhancers Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	esv2763448	chr5:29875965-29887070	Inactive region	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	n/a

No data

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

No data

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