Variant report

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs1554675	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs16842632	1.00[YRI][hapmap];0.80[AFR][1000 genomes]
rs2177693	1.00[JPT][hapmap]
rs2400443	1.00[JPT][hapmap]
rs3772645	1.00[JPT][hapmap]
rs55723894	0.85[AMR][1000 genomes]
rs55872759	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56259933	0.95[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56342381	0.80[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6439559	1.00[JPT][hapmap]
rs6772933	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6801065	1.00[JPT][hapmap]
rs6805145	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7373775	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs73862012	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7611233	1.00[JPT][hapmap]
rs7647433	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs868909	1.00[JPT][hapmap]
rs872514	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9836334	1.00[CHB][hapmap];1.00[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1000277	chr3:134546080-134970837	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv877516	chr3:134689420-134918522	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv829731	chr3:134711713-134885064	Strong transcription Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:134809200-134855200	Weak transcription	GM12878-XiMat	blood
2	chr3:134823000-134880000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr3:134834400-134846600	Weak transcription	Brain Anterior Caudate	brain
4	chr3:134840000-134842000	Strong transcription	Breast Myoepithelial Primary Cells	Breast

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