Variant report

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs1125550	0.81[ASN][1000 genomes]
rs2179217	0.84[JPT][hapmap]
rs2205945	0.92[JPT][hapmap];0.87[ASN][1000 genomes]
rs4810356	0.85[JPT][hapmap];0.81[ASN][1000 genomes]
rs4812598	0.93[JPT][hapmap];0.90[ASN][1000 genomes]
rs4812600	0.88[ASN][1000 genomes]
rs6016791	0.90[CEU][hapmap];0.94[CHB][hapmap];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6016792	0.83[ASN][1000 genomes]
rs6030212	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6030215	0.92[JPT][hapmap];0.87[ASN][1000 genomes]
rs6030216	0.85[JPT][hapmap];0.90[ASN][1000 genomes]
rs6030217	0.84[JPT][hapmap];0.90[ASN][1000 genomes]
rs6030218	0.90[CEU][hapmap];0.88[CHB][hapmap];0.84[JPT][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6030224	0.93[JPT][hapmap];0.82[ASN][1000 genomes]
rs6030226	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.95[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6030233	0.83[ASN][1000 genomes]
rs6102826	0.85[JPT][hapmap];0.90[ASN][1000 genomes]
rs6513791	0.93[JPT][hapmap];0.88[ASN][1000 genomes]
rs7268459	0.93[JPT][hapmap];0.83[ASN][1000 genomes]
rs8123429	0.82[CHB][hapmap]
rs978456	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs978457	0.91[CEU][hapmap];0.89[CHB][hapmap];0.85[JPT][hapmap];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]

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	esv2751913	chr20:40422982-41269321	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
2	nsv532516	chr20:40451059-41097155	Weak transcription Strong transcription Enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
3	nsv833987	chr20:41007663-41184914	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	9 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:41042000-41070000	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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