Variant report

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs10835892	0.83[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs10835896	0.89[CEU][hapmap]
rs11031748	0.88[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs11031755	0.88[CEU][hapmap]
rs11031762	0.89[CEU][hapmap]
rs12224661	0.81[AMR][1000 genomes]
rs2418902	0.87[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs2418905	0.80[AMR][1000 genomes]
rs3858437	0.87[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs3858439	0.80[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs5030277	0.85[CEU][hapmap]
rs5030280	0.85[CEU][hapmap]
rs5030281	0.85[CEU][hapmap]
rs5030310	0.85[CEU][hapmap]
rs56911719	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs58222320	0.81[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs58736369	0.81[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs61889189	0.80[AMR][1000 genomes]
rs7101933	0.87[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs7105549	0.81[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs7925851	0.89[CEU][hapmap];0.86[JPT][hapmap]
rs7939496	0.86[CEU][hapmap];0.86[JPT][hapmap]
rs7951745	0.88[CEU][hapmap];0.85[JPT][hapmap]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3403524	chr11:32387376-32392574	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:32375800-32387600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr11:32386800-32387600	Active TSS	K562	blood

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