Variant report

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs10048914	1.00[JPT][hapmap]
rs10511195	1.00[CHB][hapmap]
rs10937024	1.00[CHB][hapmap]
rs11714669	1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[YRI][hapmap]
rs11720144	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12054046	1.00[CHB][hapmap]
rs12233481	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs13315672	1.00[JPT][hapmap]
rs1435204	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1473269	0.81[CEU][hapmap];1.00[JPT][hapmap];0.87[EUR][1000 genomes]
rs16845024	1.00[CHB][hapmap]
rs16845027	1.00[CHB][hapmap]
rs16845049	1.00[CHB][hapmap]
rs17820915	1.00[JPT][hapmap]
rs17822800	1.00[JPT][hapmap]
rs17822848	1.00[JPT][hapmap]
rs1967598	0.87[EUR][1000 genomes]
rs2013942	1.00[CHB][hapmap]
rs2164264	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs3891857	1.00[JPT][hapmap];0.81[EUR][1000 genomes]
rs62272477	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6784362	1.00[CHB][hapmap]
rs6784389	1.00[CHB][hapmap]
rs6784826	1.00[JPT][hapmap]
rs7626999	1.00[CHB][hapmap]
rs7646053	1.00[CHB][hapmap]
rs7653110	1.00[CHB][hapmap]
rs9290704	1.00[JPT][hapmap];0.83[EUR][1000 genomes]
rs9852572	1.00[JPT][hapmap]
rs9859640	1.00[JPT][hapmap]
rs9861348	1.00[JPT][hapmap];0.87[EUR][1000 genomes]
rs9870734	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	nsv877227	chr3:102067254-102184308	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv1007340	chr3:102108954-102725099	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
3	nsv536676	chr3:102108954-102725099	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 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	chr3:102170800-102179200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr3:102177000-102179600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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