Variant report

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs1415182	0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1856049	0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1892080	0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2184837	0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs36056502	0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72761511	0.96[ASN][1000 genomes]
rs72761513	0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72761518	0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72761520	0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72761521	0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72761523	0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72761524	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72761527	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72761529	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72761530	0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72761531	0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72761532	0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72761533	0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72761535	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72761536	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7414883	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv873167	chr1:214950361-215116947	Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv873168	chr1:214962771-215064388	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:215002000-215019600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr1:215012400-215019400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr1:215012600-215021000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr1:215013000-215021000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr1:215017200-215020200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr1:215017400-215019800	Weak transcription	NHDF-Ad	bronchial
7	chr1:215017600-215020800	Weak transcription	Muscle Satellite Cultured Cells	--

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