Variant report

Variant	rs2167310
Chromosome Location	chr8:90274498-90274499
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs10955982	0.83[AMR][1000 genomes]
rs11985299	1.00[CEU][hapmap]
rs12543673	0.80[ASN][1000 genomes]
rs12544184	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[YRI][hapmap];0.92[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs12544284	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.90[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs12544420	0.88[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12544874	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[YRI][hapmap];0.90[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs12547629	0.80[AMR][1000 genomes]
rs12548260	0.83[AFR][1000 genomes];0.90[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs12676723	0.82[AMR][1000 genomes]
rs12680830	0.90[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12681083	0.81[AMR][1000 genomes]
rs1479907	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1483370	0.81[AMR][1000 genomes]
rs1483371	0.81[AMR][1000 genomes]
rs16893311	1.00[CEU][hapmap]
rs16893577	0.86[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs16893581	0.88[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1905320	0.89[ASN][1000 genomes]
rs28463376	0.93[ASN][1000 genomes]
rs35282997	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs59583486	0.88[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs59776336	0.90[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs62532521	0.83[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs62532535	0.85[AFR][1000 genomes];0.90[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs62532536	0.92[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs62532541	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6469928	0.96[ASN][1000 genomes]
rs6469929	0.94[ASN][1000 genomes]
rs6988132	0.81[AMR][1000 genomes]
rs6999851	0.83[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7013541	0.81[AMR][1000 genomes]
rs7015077	0.93[ASN][1000 genomes]
rs7817834	0.90[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7833317	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7835496	1.00[CEU][hapmap]
rs9642853	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv465735	chr8:89760311-90729507	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
2	nsv611714	chr8:89760311-90729507	Enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Weak transcription Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
3	nsv1024956	chr8:90104423-90459539	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
4	nsv539671	chr8:90104423-90459539	Active TSS Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
5	nsv1032886	chr8:90253748-90398240	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:90267200-90281200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr8:90273400-90275200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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