Variant report

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

rs_ID	r²[population]
rs13015590	1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16847650	1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16847657	1.00[YRI][hapmap]
rs16847714	0.89[YRI][hapmap];0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16847732	0.89[YRI][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16847752	0.89[YRI][hapmap]
rs16847762	0.89[YRI][hapmap]
rs16847767	0.89[YRI][hapmap]
rs16847769	0.89[YRI][hapmap]
rs16847773	0.89[YRI][hapmap]
rs16847776	0.89[YRI][hapmap]
rs16847781	1.00[YRI][hapmap]
rs57924179	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60944259	0.83[AFR][1000 genomes]
rs73987224	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73987225	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73987226	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73987229	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73987231	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73987234	0.83[AFR][1000 genomes]
rs73987235	0.81[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1011572	chr2:212840066-213152279	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
2	nsv875798	chr2:212852669-212961992	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv875802	chr2:212867291-213004603	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv875803	chr2:212874828-212969560	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv875804	chr2:212891401-212997024	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
6	nsv875805	chr2:212891401-213164837	Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	2 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	chr2:212942800-212943200	Flanking Active TSS	Dnd41	blood
2	chr2:212942800-212943400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr2:212942800-212943400	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr2:212943000-212943400	Active TSS	GM12878-XiMat	blood

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